Inhibition Of Raf Kinase Using Quinolyl, Isoquinolyl Or Pyridyl Ureas

ABSTRACT

This invention relates to a group of quinolyl, isoquinolyl and pyridyl ureas, their the use in treating raf mediated diseases, and pharmaceutical compositions which contain these ureas for use in such therapy.

This application is a continuation of U.S. non-provisional application Ser. No. 10/125,369, filed Apr. 19, 2002, which claims the benefit of U.S. provisional application No. 60/367,376 filed Apr. 20, 2001. The contents of U.S. non-provisional application Ser. No. 10/125,369 filed Apr. 19, 2002 and U.S. provisional application No. 60/367,376, filed Apr. 20, 2001 are incorporated by reference herein.

FIELD OF THE INVENTION

This invention relates to the use of a group of aryl ureas in treating raf mediated diseases, and pharmaceutical compositions for use in such therapy.

BACKGROUND OF THE INVENTION

The p21^(ras) oncogene is a major contributor to the development and progression of human solid cancers and is mutated in 30% of all human cancers (Bolton et al. Ann. Rep. Med. Chem. 1994, 29, 165-74; Bos. Cancer Res. 1989, 49, 4682-9). In its normal, unmutated form, the ras protein is a key element of the signal transduction cascade directed by growth factor receptors in almost all tissues (Avruch et al. Trends Biochem. Sci. 1994, 19, 279-83). Biochemically, ras is a guanine nucleotide binding protein, and cycling between a GTP-bound activated and a GDP-bound resting form is strictly controlled by ras' endogenous GTPase activity and other regulatory proteins. In the ras mutants in cancer cells, the endogenous GTPase activity is alleviated and, therefore, the protein delivers constitutive growth signals to downstream effectors such as the enzyme raf kinase. This leads to the cancerous growth of the cells which carry these mutants (Magnuson et al. Semin. Cancer Biol. 1994, 5, 247-53). It has been shown that inhibiting the effect of active ras by inhibiting the raf kinase signaling pathway by administration of deactivating antibodies to raf kinase or by co-expression of dominant negative raf kinase or dominant negative MEK, the substrate of raf kinase, leads to the reversion of transformed cells to the normal growth phenotype (see: Daum et al. Trends Biochem. Sci. 1994, 19, 474-80; Fridman et al. J. Biol. Chem. 1994, 269, 30105-8. Kolch et al. (Nature 1991, 349, 426-28) have further indicated that inhibition of raf expression by antisense RNA blocks cell proliferation in membrane-associated oncogenes. Similarly, inhibition of raf kinase (by antisense oligodeoxynucleotides) has been correlated in vitro and in vivo with inhibition of the growth of a variety of human tumor types (Monia et al., Nat. Med. 1996, 2, 668-75).

SUMMARY OF THE INVENTION

The present invention provides compounds which are inhibitors of the enzyme raf kinase. Since the enzyme is a downstream effector of p21^(ras), the instant inhibitors are useful in pharmaceutical compositions for human or veterinary use where inhibition of the raf kinase pathway is indicated, e.g., in the treatment of tumors and/or cancerous cell growth mediated by raf kinase. In particular, the compounds are useful in the treatment of human or animal, e.g., murine cancer, since the progression of these cancers is dependent upon the ras protein signal transduction cascade and therefore susceptible to treatment by interruption of the cascade, i.e., by inhibiting raf kinase. Accordingly, the compounds of the invention are useful in treating solid cancers, such as, for example, carcinomas (e.g., of the lungs, pancreas, thyroid, bladder or colon, myeloid disorders (e.g., myeloid leukemia) or adenomas (e.g., villous colon adenoma).

The present invention, therefore, provides compounds generally described as aryl ureas, including both aryl and heteroaryl analogues, which inhibit the raf pathway. The invention also provides a method for treating a raf mediated disease state in humans or mammals. Thus, the invention is directed to compounds which inhibit the enzyme RAF kinase and also to compounds, compositions and methods for the treatment of cancerous cell growth mediated by raf kinase wherein a compound of one of the formulae I, II or III, or a pharmaceutically acceptable salt thereof, is administered.

A-D-B  (I)

A′-D-B′  (II)

A″D-B″  (III)

In formulae I-III,

D is —NH—C(O)—NH—,

A is selected from the group consisting of substituted or unsubstituted t-butylpyridyl groups, (trifluoromethyl) pyridyl groups, isopropylpyridyl groups, (2-methyl-2-butyl)pyridyl groups, (3-methyl-3-pentyl)pyridyl groups and (3-ethyl-3-pentyl)pyridyl groups,

A′ is a substituted isoquinolinyl group or unsubstituted isoquinolinyl group or an unsubstituted quinolinyl group,

A″ is a substituted quinolinyl group,

B and B′ are each, independently, a substituted or unsubstituted bridged cyclic structure of up to 30 carbon atoms of the formula -L-(ML¹)_(q) wherein L comprises a cyclic moiety having at least 5 members and is bound directly to D, L¹ comprises a cyclic moiety having at least 5 members, M is a bridging group having at least one atom, q is an integer of from 1-3, and each cyclic structure of L and L¹ contains 0-4 members of the group consisting of nitrogen, oxygen and sulfur,

subject to the provisos that B is not

and B′ is not

B″ is a substituted or unsubstituted, up to tricyclic aryl or heteroaryl moiety of up to 30 carbon atoms with a cyclic structure bound directly to D containing at least 5 members with 0-4 members of the group consisting of nitrogen, oxygen and sulfur.

The moiety B″ is preferably either a substituted or unsubstituted bridged cyclic structure of up to 30 carbon atoms of the formula -L-(ML¹)_(q), a substituted or unsubstituted 6 member cyclic aryl moiety or 5 membered hetaryl moiety or a substituted or unsubstituted fused aryl ring or hetaryl ring of from 2-3 fused rings. For Example, B″ can be phenyl, substituted phenyl, napthyl substituted napthyl, pyridinyl, substituted pyridinyl, pyrimidinyl, substituted pyrimidinyl, quinolinyl, substituted quinolinyl, isoquinolinyl, substituted isoquinolinyl or of the formula -L(ML¹)_(q).

The substituents for A″ and the substituted isoquinolinyl groups of A′ are selected from the group consisting of halogen, up to per-halo, and Wn, where n is 0-3 and each W is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, at least a five membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, a substituted C₃₋₁₀ cycloalkyl having at least 5 cyclic members and 0-3 heteroatoms selected from N, S and O; C₆-C₁₄ aryl, C₇-C₂₄ alkaryl, C₇-C₂₄ aralkyl, C₃-C₁₂ heteroaryl having 1-3 heteroatoms selected from O, N and S, C₄-C₂₃ alkheteroaryl having 1-3 heteroatoms selected from O, N and S, up to per halo substituted C₆-C₁₂ aryl, up to per halo substituted C₃-C₁₂ hetaryl having at least 5-members and 1-3 heteroatoms selected from O, N and S, up to per halo substituted C₇-C₂₄ aralkyl, up to per halo substituted C₇-C₂₄ alkaryl, up to per halo substituted C₄-C₂₃ alkheteroaryl having at least 5 cyclic members and 1-3 heteroatoms selected from O, N and S, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ alkenyl and up to per halosubstituted C₁₋₁₀ alkenoyl.

The substituents for the substituted t-butylpyridyl, (trifluoromethyl)pyridyl, isopropylpyridyl, (2-methyl-2-butyl)pyridyl, (3-methyl-3-pentyl)pyridyl groups and (3-ethyl-3-pentyl)pyridyl groups, of A are selected from the group consisting of halogen, up to per-halo, and Zn, where n is 0-3 and each Z is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above.

Where B, B′ and B″ are substituted, the substituents are selected from the group consisting of halogen, up to per-halo, and Jn, where n is 0-3 and each J is independently selected from the group consisting of —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₃₋₁₀ cycloalkyl having at least five cyclic members and 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, C₆₋₁₂ aryl, C₃₋₁₂ hetaryl having at least five cyclic members and 1-3 heteroatoms selected from N, S and O, C₇₋₂₄ aralkyl, C₇₋₂₄ alkaryl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, substituted C₃₋₁₀ cycloalkyl having at least five cyclic members and 0-3 heteroatoms selected from N, S and O, substituted C₆-C₁₄ aryl, substituted C₃₋₁₂ hetaryl having at least five cyclic members and 1-3 heteroatoms selected from N, S and O, substituted C₇₋₂₄ alkaryl, substituted C₇-C₂₄ aralkyl and -Q-Ar, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), —C(O)NR^(a)R^(b) and —SO₂R^(a) wherein R^(a) and R^(b) are each, independently, hydrogen or a carbon based moiety of tip to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O.

R^(a) and R^(b) are preferably C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, C₆₋₁₂ aryl, C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, C₇₋₂₄ aralkyl, C₇₋₂₄ alkaryl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O, substituted C₆-C₁₄ aryl, substituted C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, substituted C₇₋₂₄ alkaryl or substituted C₇-C₂₄ aralkyl, where R^(a) is a substituted group, it is substituted by halogen up to per halo.

Where B″ of Formula III is a substituted pyridyl, substituted quinolinyl or isoquinolinyl group, B″ is preferably substituted 1 to 3 times by 1 or more substituents selected from the group consisting of —CN, halogen, C₁-C₁₀ alkyl, C₁-C₁₀ alkoxy, —OH, up to per halo substituted C₁-C₁₀ alkyl, up to per halo substituted C₁-C₁₀ alkoxy or phenyl substituted by halogen up to per halo.

Where J is a substituted group, it is substituted by halogen, up to per halo, or by one or more substituents independently selected from the group consisting of —CN, —CO₂R⁷, —OR⁷, —SR⁷, —NR⁷R^(7′), —NO₂, —NR⁷C(O)R^(7′), —NR⁷C(O)OR⁷; with each R⁷ and R^(7′) independently as defined above.

Where the substituents for B, B′ and B″ are -Q-Ar, Q is —O—, —S—, —N(R⁷)—, —(CH₂)_(m)—, —C(O)—, —O—[C(R⁹)(R^(9′))]_(m)—, —CH(OH)—, —(CH₂)_(m)O—, —(CH₂)_(m)S—, —(CH₂)_(m)N(R⁷)—, —O(CH₂)_(m)—, —CHX^(a)—, —CX^(a) ₂—, —S—(CH₂)_(m) and —N(R⁷)(CH₂)_(m), where m=1-3, R⁹ and R^(9′) are each, independently, hydrogen, C₁-C₄ alkyl and halogen, and X^(a) is halogen and each R⁷ is as defined above, and

Ar is a 5- or 6-member aromatic structure. This aromatic structure of Ar

-   -   a) contains 0-2 members selected from the group consisting of         nitrogen, oxygen and sulfur,     -   b) is free of the substituents —C(O)R^(a), —C(NR^(a))R^(b),         —C(O)NR^(a)R^(b), and —SO₂R^(a), wherein R^(a) and R^(b) are as         defined above;     -   c) is optionally substituted by halogen, up to per-halo, and     -   d) is optionally substituted by Mp, wherein p is 0 to 3 and each         M is independently selected from the group consisting of —CN,         —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)(O)R^(7′), —NR⁷C(O)R^(7′),         with each R⁷ and R^(7′) independently as defined above, C₁₋₁₀         alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl and C₁₋₁₀ alkenoyl halo         substituted C₁₋₁₀ alkyl up to per halo, halo substituted C₁₋₁₀         alkoxy up to per halo, halosubstituted C₂₋₁₀ alkenyl up to per         halo and halosubstituted C₁₋₁₀ alkenoyl up to per halo.

The bridging group M in the formula -L-(ML¹)_(q), for B, B′ and B″ is preferably selected from the group consisting of —O—, —S—, —N(R⁷)—, —(CH₂)_(m)—, —C(O)—, —CH(OH)—, —(CH₂)_(m)O—, —(CH₂)_(m)S—, —(CH₂)_(m) N(R⁷)—, —O(CH₂)_(m)—CHX^(a)—, —CX^(a) ₂—, S—(CH₂)_(m)— and —N(R⁷)(CH₂)_(m), where m=1-3, X^(a) is hydrogen and R⁷ is as defined above and q is 1. More preferably, M is —O—, —CH₂—, —S—, —NH—, —C(O)—, —O—CH₂— and —CH₂—O—.

The moieties L and L¹ in the formula -L-(ML¹)_(q) for B, B′ and B″ are typically each, independently, a substituted aryl moiety having at least 6 cyclic members, a substituted hetaryl moiety having at least 5 cyclic members, an substituted aryl moiety having at least 6 cyclic members or an unsubstituted hetaryl moiety having at least 5 cyclic members. The hetaryl moieties for L and L′ typically have 1 to 4 members selected from the group of hetaryl atoms consisting of nitrogen, oxygen and sulfur with the balance of the hetaryl moiety being carbon. More typical moieties for L¹ and L are selected from the group consisting of thiophene, phenyl, substituted phenyl, pyridinyl, substituted pyridinyl, pyrimidinyl substituted pyrimidinyl quinolyl, substituted quinolyl isoquinolyl, substituted isoquinolyl, napthyl and substituted napthyl.

The substituted t-butylpyridyls, (trifluoromethyl)pyridyls, isopropylpyridyls, (2-methyl-2-butyl)pyridyls, (3-methyl-3-pentyl)pyridyls and (3-ethyl-3-pentyl)pyridyls of A, the substituted isoquinolinyls of A′ and the substituted quinolinyls of A″ preferably have 1-3 substituents selected from the group consisting of C₁₋₁₀ alkyl, up to per halo substituted C₁₋₁₀alkyl, —CN, —OH, halogen, C₁₋₁₀ alkoxy, up to per halo substituted C₁₋₁₀ alkoxy and C3-C10 heterocyclic moieties comprising 1 to 2 heteroatoms selected from the group of consisting of nitrogen, oxygen and sulfur.

Preferred compounds of Formula I include those wherein the cyclic structures of B and L bound directly to D are not substituted in the ortho position by —OH.

In Formulae I, II and III suitable hetaryl groups include, but are not limited to, 5-12 carbon-atom aromatic rings or ring systems containing 1-3 rings, at least one of which is aromatic, in which one or more, e.g., 1-4 carbon atoms in one or more of the rings can be replaced by oxygen, nitrogen or sulfur atoms. Each ring typically has 3-7 atoms. For example, B can be 2- or 3-furyl, 2- or 3-thienyl, 2- or 4-triazinyl, 1-, 2- or 3-pyrrolyl, 1-, 2-, 4- or 5-imidazolyl, 1-, 3-, 4- or 5-pyrazolyl, 2-, 4- or 5-oxazolyl, 3-, 4- or 5-isoxazolyl, 2-, 4- or 5-thiazolyl, 3-, 4- or 5-isothiazolyl, 2-, 3- or 4-pyridyl, 2-, 4-, 5- or 6-pyrimidinyl, 1,2,3-triazol-1-, -4- or -5-yl, 1,2,4-triazol-1-, -3- or -5-yl, 1- or 5-tetrazolyl, 1,2,3-oxadiazol-4- or -5-yl, 1,2,4-oxadiazol-3- or -5-yl, 1,3,4-thiadiazol-2- or -5-yl, 1,2,4-oxadiazol-3- or -5-yl, 1,3,4-thiadiazol-2- or -5-yl, 1,3,4-thiadiazol-3- or -5-yl, 1,2,3-thiadiazol-4- or -5-yl, 2-, 3-, 4-, 5- or 6-2H-thiopyranyl, 2-, 3- or 4-4H-thiopyranyl, 3- or 4-pyridazinyl, pyrazinyl, 2-, 3-, 4-, 5-, 6- or 7-benzofuryl, 2-, 3-, 4-, 5-, 6- or 7-benzothienyl, 1-, 2-, 3-, 4-, 5-, 6- or 7-indolyl, 1-, 2-, 4- or 5-benzimidazolyl, 1-, 3-, 4-, 5-, 6- or 7-benzopyrazolyl, 2-, 4-, 5-, 6- or 7-benzoxazolyl, 3-, 4-, 5-6- or 7-benzisoxazolyl, 1-, 3-, 4-, 5-, 6- or 7-benzothiazolyl, 2-, 4-, 5-, 6- or 7-benzisothiazolyl, 2-, 4-, 5-, 6- or 7-benz-1,3-oxadiazolyl, 2-, 3-, 4-, 5-, 6-, 7- or 8-quinolinyl, 1-, 3-, 4-, 5-, 6-, 7-, 8-isoquinolinyl, 1-, 2-, 3-, 4- or 9-carbazolyl, 1-, 2-, 3-, 4-, 5-, 6-, 7-, 8- or 9-acridinyl, or 2-, 4-, 5-, 6-, 7- or 8-quinazolinyl, or additionally optionally substituted phenyl, 2- or 3-thienyl, 1,3,4-thiadiazolyl, 3-pyrryl, 3-pyrazolyl, 2-thiazolyl or 5-thiazolyl, etc. For example, B can be 4-methyl-phenyl, 5-methyl-2-thienyl, 4-methyl-2-thienyl, 1-methyl-3-pyrryl, 1-methyl-3-pyrazolyl, 5-methyl-2-thiazolyl or 5-methyl-1,2,4-thiadiazol-2-yl.

Suitable alkyl groups and alkyl portions of groups, e.g., alkoxy, etc. throughout include methyl, ethyl, propyl, butyl, etc., including all straight-chain and branched isomers such as isopropyl, isobutyl, sec-butyl, tert-butyl, etc.

Suitable aryl groups which do not contain heteroatoms include, for example, phenyl and 1- and 2-naphthyl.

The term “cycloalkyl”, as used herein, refers to cyclic structures with or without alkyl substituents such that, for example, “C₄ cycloalkyl” includes methyl substituted cyclopropyl groups as well as cyclobutyl groups. The term “cycloalkyl”, as used herein also includes saturated heterocyclic groups.

Suitable halogen groups include F, Cl, Br, and/or I, from one to per-substitution (i.e. all H atoms on a group replaced by a halogen atom) being possible where an alkyl group is substituted by halogen, mixed substitution of halogen atom types also being possible on a given moiety.

The invention also relates to compounds per se, of formula I, II and III.

The present invention is also directed to pharmaceutically acceptable salts of formulae I, II and III. Suitable pharmaceutically acceptable salts are well known to those skilled in the art and include basic salts of inorganic and organic acids, such as hydrochloric acid, hydrobromic acid, sulphuric acid, phosphoric acid, methanesulphonic acid, trifluoromethanesulfonic acid, benzenesulphonic acid, p-toluenesulfonic acid, 1-naphthalenesulfonic acid, 2-naphthalenesulfonic acid, acetic acid, trifluoroacetic acid, malic acid, tartaric acid, citric acid, lactic acid, oxalic acid, succinic acid, fumaric acid, maleic acid, benzoic acid, salicylic acid, phenylacetic acid, and mandelic acid. In addition, pharmaceutically acceptable salts include acid salts of inorganic bases, such as salts containing alkaline cations (e.g., Li⁺ Na⁺ or K⁺), alkaline earth cations (e.g., Mg⁺², Ca⁺² or Ba⁺²), the ammonium cation, as well as acid salts of organic bases, including aliphatic and aromatic substituted ammonium, and quaternary ammonium cations, such as those arising from protonation or peralkylation of triethylamine, N,N-diethylamine, N,N-dicyclohexylamine, lysine, pyridine, N,N-dimethylaminopyridine (DMAP), 1,4-diazabiclo[2.2.2]octane (DABCO), 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).

A number of the compounds of Formula I, II and III possess asymmetric carbons and can therefore exist in racemic and optically active forms. Methods of separation of enantiomeric and diastereomeric mixtures are well known to one skilled in the art. The present invention encompasses any racemic or optically active form of compounds described in Formulae I, II and III which possess progesterone receptor binding activity.

General Preparative Methods

The compounds of Formulae I, II and III may be prepared by the use of known chemical reactions and procedures, some from starting materials which are commercially available. Nevertheless, general preparative methods are provided below to aid one skilled in the art in synthesizing these compounds, with more detailed examples being provided in the Experimental section which follows.

Substituted and unsubstituted aminoquinolines, aminoisoquinolines and aminopyridines may be prepared using standard methods (see, for example: A. R. Katritzky et al. (Eds.). Comprehensive Heterocyclic Chemistry II, Vol. 5. M. H. Palmer. Heterocyclic Compounds; Arnold Ltd., London (1967). C. K. Esser et al. WO 96/18616. C. J. Donahue et al. Inorg. Chem. 30, 1991, 1588. E. Cho et al. WO 98/00402. A. Cordi et al. Bioorg Med. Chem. 3, 1995, 129). In addition, many aminoquinolines, aminoisoquinolines and aminopyridines are commercially available.

Substituted anilines may be generated using standard methods (March. Advanced Organic Chemistry, 3^(rd) Ed.; John Wiley: New York (1985). Larock. Comprehensive Organic Transformations; VCH Publishers: New York (1989)). As shown in Scheme I, aryl amines are commonly synthesized by reduction of nitroaryls using a metal catalyst, such as Ni, Pd, or Pt, and H₂ or a hydride transfer agent, such as formate, cyclohexadiene, or a borohydride (Rylander. Hydrogenation Methods; Academic Press: London, UK (1985)). Nitroaryls may also be directly reduced using a strong hydride source, such as LiAlH₄ (Seyden-Penne. Reductions by the Alumino- and Borohydrides in Organic Synthesis; VCH Publishers: New York (1991)), or using a zero valent metal, such as Fe, Sn or Ca, often in acidic media. Many methods exist for the synthesis of nitroaryls (March. Advanced Organic Chemistry, 3^(rd) Ed.; John Wiley. New York (1985). Larock. Comprehensive Organic Transformations; VCH Publishers: New York (1989)).

Nitroaryls are commonly formed by electrophilic aromatic nitration using HNO₃, or an alternative NO₂ ⁺ source. Nitroaryls may be further elaborated prior to reduction. Thus, nitroaryls substituted with

potential leaving groups (e.g. F, Cl, Br, etc.) may undergo substitution reactions on treatment with nucleophiles, such as thiolate (exemplified in Scheme II) or phenoxide. Nitroaryls may also undergo Ullman-type coupling reactions (Scheme II).

Nitroaryls may also undergo transition metal mediated cross coupling reactions. For example, nitroaryl electrophiles, such as nitroaryl bromides, iodides or triflates, undergo palladium mediated cross coupling reactions with aryl nucleophiles, such as arylboronic acids (Suzuki reactions, exemplified below), aryltins (Stille reactions) or arylzincs (Negishi reaction) to afford the biaryl (5).

Either nitroaryls or anilines may be converted into the corresponding arenesulfonyl chloride (7) on treatment with chlorosulfonic acid. Reaction of the sulfonyl chloride with a fluoride source, such as KF then affords sulfonyl fluoride (8). Reaction of sulfonyl fluoride 8 with trimethylsilyl trifluoromethane in the presence of a fluoride source, such as tris(dimethylamino)sulfonium difluorotrimethylsiliconate (TASF) leads to the corresponding trifluoromethylsulfone (9). Alternatively, sulfonyl chloride 7 may be reduced to the arenethiol (10), for example with zinc amalgum. Reaction of thiol 10 with CHClF₂ in the presence of base gives the difluoromethyl mercaptan (11), which may be oxidized to the sulfone (12) with any of a variety of oxidants, including CrO₃-acetic anhydride (Sedova et al. Zh. Org. Khim. 1970, 6, (568),

As shown in Scheme IV, non-symmetrical urea formation may involve reaction of an aryl isocyanate (14) with an aryl amine (13). The heteroaryl isocyanate may be synthesized from a heteroaryl amine by treatment with phosgene or a phosgene equivalent, such as trichloromethyl chloroformate (diphosgene), bis(trichloromethyl) carbonate (triphosgene) or N,N′-carbonyldiimidazole (CDI). The isocyanate may also be derived from a heterocyclic carboxylic acid derivative, such as an ester, an acid halide or an anhydride by a Curtius-type rearrangement. Thus, reaction of acid derivative 16 with an azide source, followed by rearrangement affords the isocyanate. The corresponding carboxylic acid (17) may also be subjected to Curtius-type rearrangements using dephenylphosphoryl axide (DPPA) or a similar reagent.

Finally, ureas may be further manipulated using methods familiar to those skilled in the art.

The invention also includes pharmaceutical compositions including at least one compound of Formula I, II or III and a physiologically acceptable carrier.

The compounds may be administered orally, dermally, parenterally, by injection, by inhalation or spray, or sublingually, rectally or vaginally in dosage unit formulations. The term ‘administration by injection’ includes intravenous, intraarticular, intramuscular, subcutaneous and parenteral injections, as well as use of infusion techniques. Dermal administration may include topical application or transdermal administration. One or more compounds may be present in association with one or more non-toxic pharmaceutically acceptable carriers and if desired other active ingredients.

Compositions intended for oral use may be prepared according to any suitable method known to the art for the manufacture of pharmaceutical compositions. Such compositions may contain one or more agents selected from the group consisting of diluents, sweetening agents, flavoring agents, coloring agents and preserving agents in order to provide palatable preparations. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets. These excipients may be, for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating, and disintegrating agents, for example, corn starch, or alginic acid; and binding agents, for example magnesium stearate, stearic acid or talc. The tablets may be uncoated or they may be coated by known techniques to delay disintegration and adsorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time delay material such as glyceryl monostearate or glyceryl distearate may be employed. These compounds may also be prepared in solid, rapidly released form.

Formulations for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin or olive oil.

Aqueous suspensions containing the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions may also be used. Such excipients are suspending agents, for example sodium carboxymethylcellulose, methylcellulose, hydroxypropyl-methylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally-occurring phosphatide, for example, lecithin, or condensation products of an alkylene oxide with fatty acids, for example polyoxyethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives, for example ethyl, or n-propyl, p-hydroxybenzoate, one or more coloring agents, one or more flavoring agents, and one or more sweetening agents, such as sucrose or saccharin.

Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water provide the active ingredient in admixture with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients, for example, sweetening, flavoring and coloring agents, may also be present.

The compounds may also be in the form of non-aqueous liquid formulations, e.g., oily suspensions which may be formulated by suspending the active ingredients in a vegetable oil, for example arachis oil, olive oil, sesame oil or peanut oil, or in a mineral oil such as liquid paraffin. The oily suspensions may contain a thickening agent, for example beeswax, hard paraffin or cetyl alcohol, Sweetening agents such as those set forth above, and flavoring agents may be added to provide palatable oral preparations. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.

Pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oil phase may be a vegetable oil, for example olive oil or arachis oil, or a mineral oil, for example liquid paraffin or mixtures of these. Suitable emulsifying agents may be naturally-occurring gums, for example gum acacia or gum tragacanth, naturally-occurring phosphatides, for example soy bean, lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides, for example sorbitan monooleate, and condensation products of the said partial esters; with ethylene oxide, for example polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening and flavoring agents.

Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative and flavoring and coloring agents.

The compounds may also be administered in the form of suppositories for rectal or vaginal administration of the drug. These compositions can be prepared by mixing the drug with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal or vaginal temperature and will therefore melt in the rectum or vagina to release the drug. Such materials include cocoa butter and polyethylene glycols.

Compounds of the invention may also be administered transdermally using methods known to those skilled in the art (see, for example: Chien; “Transdermal Controlled Systemic Medications”; Marcel Dekker Inc.; 1987. Lipp et al. WO94/04157 3 Mar. 1994). For example, a solution or suspension of a compound of Formula I in a suitable volatile solvent optionally containing penetration enhancing agents can be combined with additional additives known to those skilled in the art, such as matrix materials and bacteriocides. After sterilization, the resulting mixture can be formulated following known procedures into dosage forms. In addition, on treatment with emulsifying agents and water, a solution or suspension of a compound of Formulae I, II or III may be formulated into a lotion or salve.

Suitable solvents for processing transdermal delivery systems are known to those skilled in the art, and include lower alcohols such as ethanol or isopropyl alcohol, lower ketones such as acetone, lower carboxylic acid esters such as ethyl acetate, polar ethers such as tetrahydrofuran, lower hydrocarbons such as hexane, cyclohexane or benzene, or halogenated hydrocarbons such as dichloromethane, chloroform, trichlorotrifluoroethane, or trichlorofluoroethane. Suitable solvents may also include mixtures one or more materials selected from lower alcohols, lower ketones, lower carboxylic acid esters, polar ethers, lower hydrocarbons, halogenated hydrocarbons.

Suitable penetration enhancing materials for transdermal delivery systems are known to those skilled in the art, and include, for example, monohydroxy or polyhydroxy alcohols such as ethanol, propylene glycol or benzyl alcohol, saturated or unsaturated C₈-C₁₈ fatty alcohols such as lauryl alcohol or cetyl alcohol, saturated or unsaturated C₈-C₁₈ fatty acids such as stearic acid, saturated or unsaturated fatty esters with up to 24 carbons such as methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl isobutyl tert-butyl or monoglycerin esters of acetic acid, capronic acid, lauric acid, myristinic acid, stearic acid, or palmitic acid, or diesters of saturated or unsaturated dicarboxylic acids with a total of up to 24 carbons such as diisopropyl adipate, diisobutyl adipate, diisopropyl sebacate, diisopropyl maleate, or diisopropyl fumarate. Additional penetration enhancing materials include phosphatidyl derivatives such as lecithin or cephalin, terpenes, amides, ketones, ureas and their derivatives, and ethers such as dimethyl isosorbid and diethyleneglycol monoethyl ether. Suitable penetration enhancing formulations may also include mixtures one or more materials selected from monohydroxy or polyhydroxy alcohols, saturated or unsaturated C₈-C₁₈ fatty alcohols, saturated or unsaturated C₈-C₁₈ fatty acids, saturated or unsaturated fatty esters with up to 24 carbons, diesters of saturated or unsaturated dicarboxylic acids with a total of up to 24 carbons, phosphatidyl derivatives, terpenes, amides, ketones, ureas and their derivatives, and ethers.

Suitable binding materials for transdermal delivery systems are known to those skilled in the art and include polyacrylates, silicones, polyurethanes, block polymers, styrene-butadiene copolymers, and natural and synthetic rubbers. Cellulose ethers, derivatized polyethylenes, and silicates may also be used as matrix components. Additional additives, such as viscous resins or oils may be added to increase the viscosity of the matrix.

For all regimens of use disclosed herein for compounds of Formulae I, II and III, the daily oral dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily dosage for administration by injection, including intravenous, intramuscular, subcutaneous and parenteral injections, and use of infusion techniques will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily rectal dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily vaginal dosage regimen will preferably be from 0.01 to 200 mg/Kg of total body weight. The daily dosages for oral administration, administration by injection, rectal administration and vaginal administration can be achieved by multiple administrations per day or by administration as infrequently as once every 14 days. The long term dosage, can range from 100-800 mg/Kg of total body weight, more preferably 200-600 mg/Kg of total body weight. The daily topical dosage regimen will preferably be from 0.1 to 200 mg administered between one to four times daily. The transdermal concentration will preferably be that required to maintain a daily dose of from 0.01 to 200 mg/Kg of total body weight. The daily inhalation dosage regimen will preferably be from 0.01 to 10 mg/Kg of total body weight.

It will be appreciated by those skilled in the art that the particular method of administration will depend on a variety of factors, all of which are considered routinely when administering therapeutics. It will also be understood, however, that the specific dose level for any given patient will depend upon a variety of factors, including, but not limited to the activity of the specific compound employed, the age of the patient, the body weight of the patient, the general health of the patient, the gender of the patient, the diet of the patient, time of administration, route of administration, rate of excretion, drug combinations, and the severity of the condition undergoing therapy. It will be further appreciated by one skilled in the art that the optimal course of treatment, i.e., the mode of treatment and the daily or weekly number of doses of a compound of Formulae I, II or III or a pharmaceutically acceptable salt thereof given for a defined number of days, can be ascertained by those skilled in the art using conventional treatment tests.

The entire disclosure of all applications, patents and publications cited above and below are hereby incorporated by reference.

The compounds of Figure I, II and III are producible from known compounds (or from starting materials which, in turn, are producible from known compounds), e.g., through the general preparative methods shown below. The activity of a given compound to inhibit raf kinase can be routinely assayed, e.g., according to procedures disclosed below. The following examples are for illustrative purposes only and are not intended, nor should they be construed to limit the invention in any way.

EXAMPLES

All reactions were performed in flame-dried or oven-dried glassware under a positive pressure of dry argon or dry nitrogen, and were stirred magnetically unless otherwise indicated. Sensitive liquids and solutions were transferred via syringe or cannula, and introduced into reaction vessels through rubber septa. Unless otherwise stated, the term ‘concentration under reduced pressure’ refers to use of a Buchi rotary evaporator at approximately 15 mmHg. Unless otherwise stated, the term ‘under high vacuum’ refers to a vacuum of 0.4-1.0 mmHg.

All temperatures are reported uncorrected in degrees Celsius (° C.). Unless otherwise indicated, all parts and percentages are by weight.

Commercial grade reagents and solvents were used without further purification. N-cyclohexyl-N′-(methylpolystyrene)carbodiimide was purchased from Calbiochem-Novabiochem Corp. 5-(Trifluoromethyl)-2-aminopyridine, 3-aminoquinioline, 3-aminoisoquinoline, 1-(4-methylpiperazinyl)-3-aminoisoquinoline, ethyl 4-isocyanatobenzoate, N-acetyl-4-chloro-2-methoxy-5-(trifluoromethyl)aniline, 4-(4-nitrobenzyl)pyridine, 4-phenoxyaniline, 4-(4-methylphenoxy)aniline, 4-(4-chlorophenoxy)aniline and 4-chloro-3-(trifluoromethyl)phenyl isocyanate were purchased and used without further purification. Syntheses of 2-amino-4-tert-butylpyridine (C. K. Esser et al. WO 96/18616; C. J. Donahue et al. Inorg. Chem. 30, 1991, 1588), 3-amino-2-methoxyquinoline (E. Cho et al. WO 98/00402; A. Cordi et al. EP 542,609; IBID Bioorg. Med. Chem. 3, 1995, 129), 4-(3-carbamoylphenoxy)-1-nitrobenzene (K. Ikawa Yakugaku Zasshi 79, 1959, 760; Chem, Abstr. 53, 1959, 12761b), 4-[(4-methoxyphenyl)methylamino]aniline (P. Brenneisen et al. U.S. Pat. No. 3,755,406; IBID U.S. Pat. No. 3,839,582; IBID DE 1,935,388), 4-(4-pyridylcarbonyl)aniline (M. L. Carmello et al. Pestic. Sci. 45, 1995, 227), 3-tert-butylphenyl isocyanate (O. Rohr et al. DE 2,436,108) and 2-methoxy-5-(trifluoromethyl)phenyl isocyanate (K. Inukai et al. JP 42,025,067; IBID Kogyo Kagaku Zasshi 70, 1967, 491) have previously been described.

Thin-layer chromatography (TLC) was performed using Whatman® pre-coated glass-backed silica gel 60A F-254 250 μm plates. Visualization of plates was effected by one or more of the following techniques: (a) ultraviolet illumination, (b) exposure to iodine vapor, (c) immersion of the plate in a 10% solution of phosphomolybdic acid in ethanol followed by heating, (d) immersion of the plate in a cerium sulfate solution followed by heating, and/or (e) immersion of the plate in an acidic ethanol solution of 2,4-dinitrophenylhydrazine followed by heating. Column chromatography (flash chromatography) was performed using 230-400 mesh EM Science® silica gel.

Melting points (mp) were determined using a Thomas-Hoover melting point apparatus or a Mettler FP66 automated melting point apparatus and are uncorrected. Fourier transform infrared spectra were obtained using a Mattson 4020 Galaxy Series spectrophotometer. Proton (¹H) nuclear magnetic resonance (NMR) spectra were measured with a General Electric GN-Omega 300 (300 MHz) spectrometer with either Me₄Si (δ 0.00) or residual protonated solvent (CHCl₃ δ7.26; MeOH δ 3.30; DMSO δ 2.49) as standard. Carbon (¹³C) NMR spectra were measured with a General Electric GN-Omega 300 (75 NMz) spectrometer with solvent (CDCl₃ δ 77.0; MeOD-d₃; δ 49.0; DMSO-d₆ δ 39.5) as standard. Low resolution mass spectra (MS) and high resolution mass spectra (HRMS) were either obtained as electron impact (EI) mass spectra or as fast atom bombardment (FAB) mass spectra. Electron impact mass spectra (EI-MS) were obtained with a Hewlett Packard 5989A mass spectrometer equipped with a Vacumetrics Desorption Chemical Ionization Probe for sample introduction. The ion source was maintained at 250° C. Electron impact ionization was performed with electron energy of 70 eV and a trap current of 300 μA. Liquid-cesium secondary ion mass spectra (FAB-MS), an updated version of fast atom bombardment were obtained using a Kratos Concept 1-H spectrometer. Chemical ionization mass spectra (CI-MS) were obtained using a Hewlett Packard MS-Engine (5989A) with methane or ammonia as the reagent gas (1×10⁻⁴ torr to 2.5×10⁻⁴ torr). The direct insertion desorption chemical ionization (DCI) probe (Vacuumetrics, Inc.) was ramped from 0-1.5 amps in 10 sec and held at 10 amps until all traces of the sample disappeared (˜1-2 min). Spectra were scanned from 50-800 amu at 2 sec per scan. HPLC-electrospray mass spectra (HPLC ES-MS) were obtained using a Hewlett-Packard 1100 HPLC equipped with a quaternary pump, a variable wavelength detector, a C-18 column, and a Finnigan LCQ ion trap mass spectrometer with electrospray ionization. Spectra were scanned from 120-800 amu using a variable ion time according to the number of ions in the source. Gas chromatography—ion selective mass spectra (GC-MS) were obtained with a Hewlett Packard 5890 gas chromatograph equipped with an HP-1 methyl silicone column (0.33 mM coating; 25 m×0.2 mm) and a Hewlett Packard 5971 Mass Selective Detector (ionization energy 70 eV). Elemental analyses were conducted by Robertson Microlit Labs, Madison N.J.

All compounds displayed NMR spectra, LRMS and either elemental analysis or HRMS consistant with assigned structures.

LIST OF ABBREVIATIONS AND ACRONYMS

AcOH acetic acid anh anhydrous atm atmosphere(s) BOC tert-butoxycarbonyl CDI 1,1′-carbonyl diimidazole conc concentrated dec decomposition

DMAC N,N-dimethylacetamide

DMPU 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone

DMF N,N-dimethylformamide

DMSO dimethylsulfoxide DPPA diphenylphosphoryl azide EDCI 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide EtOAc ethyl acetate EtOH ethanol (100%) Et₂O diethyl ether Et₃N triethylamine HOBT 1-hydroxybenzotriazole m-CPBA 3-chloroperoxybenzoic acid MeOH methanol pet. ether petroleum ether (boiling range 30-60° C.) THF tetrahydrofuran TFA trifluoroacetic acid Tf trifluoromethanesulfonyl

A. General Methods for Synthesis of Substituted Anilines A1. General Method for Substituted Aniline Formation Via Hydrogenation of a Nitroarene

4-(4-Pyridinylmethyl)aniline: To a solution of 4-(4-nitrobenzyl)pyridine (7.0 g, 32.68 mmol) in EtOH (200 mL) was added 10% Pd/C (0.7 g) and the resulting slurry was shaken under a H₂ atmosphere (50 psi) using a Parr shaker. After 1 h, TLC and ¹H-NMR of an aliquot indicated complete reaction. The mixture was filtered through a short pad of Celite®. The filtrate was concentrated in vacuo to afford a white solid (5.4 g, 90%): ¹H-NMR (DMSO-d₆) δ 3.74 (s, 2H), 4.91 br s, 2H), 6.48 (d, J=8.46 Hz, 2H), 6.86 (d, J=8.09 Hz, 2H), 7.16 (d, J=5.88 Hz, 2H), 8.40 (d, J=5.88 Hz, 2H); EI-MS m/z 184 (M⁺). This material was used in urea formation reactions without further purification.

A2, General Method for Substituted Aniline Formation Via Dissolving Metal Reduction of a Nitroarene

4-(2-Pyridinylthio)aniline; To a solution of 4-(2-pyridinylthio)-1-nitrobenzene (Menai ST 3355A; 0.220 g 0.95 mmol) and H₂O (0.5 mL) in AcOH (5 mL) was added iron powder (0.317 g, 5.68 mmol) and the resulting slurry stirred for 16 h at room temp. The reaction mixture was diluted with EtOAc (75 mL) and H₂O (50 mL), basified to pH 10 by adding solid K₂CO₃ in portions (Caution: foaming). The organic layer was washed with a saturated NaCl solution, dried (MgSO₄), concentrated in vacuo. The residual solid was purified by MPLC (30% EtOAc/70% hexane) to give the desired product as a thick oil (0.135 g, 70%); TLC (30% EtOAc/70% hexanes) R_(f) 0.20.

A3a. General Method for Substituted Aniline Formation via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 1-Methoxy-4-(4-nitrophenoxy)benzene: To a suspension of NaH (95%, 1.50 g, 59 mmol) in DMF (100 mL) at room temp. was added dropwise a solution of 4-methoxyphenol (7.39 g, 59 mmol) in DMF (50 mL). The reaction was stirred 1 h, then a solution of 1-fluoro-4-nitrobenzene (7.0 g, 49 mmol) in DMF (50 mL) was added dropwise to form a dark green solution. The reaction was heated at 95° C. overnight, then cooled to room temp., quenched with H₂O and concentrated in vacuo. The residue was partitioned between EtOAc (200 mL) and H₂O (200 mL). The organic layer was sequentially washed with H₂O (2×200 mL), a saturated NaHCO₃ solution (200 mL), and a saturated NaCl solution (200 mL), dried (Na₂SO₄), and concentrated in vacuo. The residue was triturated (Et₂O/hexane) to afford t-methoxy-4-(4-nitrophenoxy)benzene (12.2 g, 100%); ¹H-NMR (CDCl₃) δ 3.83 (s, 3H), 6.93-7.04 (m, 6H), 8.18 (d, J=9.2 Hz, 2H); EI-MS m/z 245 (M⁺).

Step 2. 4-(4-Methoxyphenoxy)aniline: To a solution of 1-methoxy-4-(4-nitrophenoxy)benzene (12.0 g, 49 mmol) in EtOAc (250 mL) was added 5% Pt/C (1.5 g) and the resulting slurry was shaken under a H₂ atmosphere (50 psi) for 18 h. The reaction mixture was filtered through a pad of Celite® with the aid of EtOAc and concentrated in vacuo to give an oil which slowly solidified (10.6 g, 100%): ¹H-NMR (CDCl₃) δ 3.54 (br s, 2H), 3.78 (s, 3H), 6.65 (d, J=8.8 Hz, 2H), 6.79-6.92 (m, 6H); EI-MS m/z 215 (M⁺).

A3b. General Method for Substituted Aniline Formation Via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 3-(Trifluoromethyl)-4-(4-pyridinylthio)nitrobenzene: A solution of 4-mercaptopyridine (2.8 g, 24 mmoles), 2-fluoro-5-nitrobenzotrifluoride (5 g, 23.5 mmoles), and potassium carbonate (6.1 g, 44.3 mmoles) in anhydrous DMF (80 mL) was stirred at room temperature and under argon overnight. TLC showed complete reaction. The mixture was diluted with Et₂O (100 mL) and water (100 mL) and the aqueous layer was back-extracted with Et₂O (2×100 mL). The organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO₄), and concentrated under reduced pressure. The solid residue was triturated with Et₂O to afford the desired product as a tan solid (3.8 g, 54%): TLC (30% EtOAc/70% hexane) R_(f) 0.06; ¹H-NMR (DMSO-d₆) δ 7.33 (dd, J=1.2, 4.2 Hz, 2H), 7.78 (d, J=8.7 Hz, 1H), 8.46 (dd, J=2.4, 8.7 Hz, 1H), 8.54-8.56 (m, 3H).

Step 2. 3-(Trifluoromethyl)-4-(4-pyridinylthio)aniline: A slurry of 3-trifluoromethyl-4-(4-pyridinylthio)nitrobenzene (3.8 g, 12.7 mmol), iron powder (4.0 g, 71.6 mmol), acetic acid (100 mL), and water (1 mL) were stirred at room temp. for 4 h. The mixture was diluted with Et₂O (100 mL) and water (100 mL). The aqueous phase was adjusted to pH 4 with a 4 N NaOH solution. The combined organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO₄), and concentrated under reduced pressure. The residue was filtered through a pad of silica (gradient from 50% EtOAc/50% hexane to 60% EtOAc/40% hexane) to afford the desired product (3.3 g); TLC (50% EtOAc/50% hexane) R_(f) 0.10; ¹H-NMR (DMSO-d₆) δ 6.21 (s, 2H), 6.84-6.87 (m, 3H), 7.10 (d, J=2.4 Hz, 1H), 7.39 (d, J=8.4 Hz, 1H), 8.29 (d, J=6.3 Hz, 2H).

A3c. General Method for Substituted Aniline Formation Via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 4-(2-(4-Phenyl)thiazolyl)thio-1-nitrobenzene: A solution of 2-mercapto-4-phenylthiazole (4.0 g, 20.7 mmoles) in DMF (40 mL) was treated with 1-fluoro-4-nitrobenzene (2.3 mL, 21.7 mmoles) followed by K₂CO₃ (3.18 g, 23 mol), and the mixture was heated at approximately 65° C. overnight. The reaction mixture was then diluted with EtOAc (100 mL), sequentially washed with water (100 mL) and a saturated NaCl solution (100 mL), dried (MgSO₄) and concentrated under reduced pressure. The solid residue was triturated with a Et₂O/hexane solution to afford the desired product (6.1 g): TLC (25% EtOAc/75% hexane) R_(f) 0.49; ¹H-NMR (CDCl₃) δ 7.35-7.47 (m, 3H), 7.58-7.63 (m, 3H), 7.90 (d, J=6.9 Hz, 2H), 8.19 (d, J==9.0 Hz, 2H).

Step 2. 4-(2-(4-Phenyl)thiazolyl)thioaniline: 4-(2-(4-Phenyl)thiazolyl)thio-1-nitro-benzene was reduced in a manner analagous to that used in the preparation of 3-(trifluoromethyl)-4-(4-pyridinylthio)aniline: TLC (25% EtOAc/75% hexane) R_(f) 0.18; ¹H-NMR (CDCl₃) δ 3.89 (br s, 2H), 6.72-6.77 (m, 2H), 7.26-7.53 (m, 6H), 7.85-7.89 (m, 2H).

A3d. General Method for Substituted Aniline Formation Via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 4-(6-Methyl-3-pyridinyloxy)-1-nitrobenzene: To a solution of 5-hydroxy-2-methylpyridine (5.0 g, 45.8=mol) and 1-fluoro-4-nitrobenzene (6.5 g, 45.8 mmol) in anh DMF (50 mL) was added K₂CO₃ (13.0 g, 91.6 mmol) in one portion. The mixture was heated at the reflux temp. with stirring for 18 h and then allowed to cool to room temp. The resulting mixture was poured into water (200 mL) and extracted with EtOAc (3×150 mL). The combined organics were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na₂SO₄), and concentrated in vacuo to afford the desired product (8.7 g, 83%). This material was carried to the next step without further purification.

Step 2. 4-(6-Methyl-3-pyridinyloxy)aniline: A solution of 4-(6-methyl-3-pyridinyloxy)-1-nitrobenzene (4.0 g, 17.3 mmol) iii EtOAc (150 mL) was added to 10% Pd/C (0.500 g, 0.47 mmol) and the resulting mixture was placed under a H₂ atmosphere (balloon) and was allowed to stir for 18 h at room temp. The mixture was then filtered through a pad of Celite® and concentrated in vacuo to afford the desired product as a tan solid (3.2 g, 92%): EI-MS m/z 200 (M⁺).

A3e. General Method for Substituted Aniline Formation Via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 4-(3,4-Dimethoxyphenoxy)-1-nitrobenzene: To a solution of 3,4-dimethoxyphenol (1.0 g, 6.4 mmol) and 1-fluoro-4-nitrobenzene (700 μL, 6.4 mmol) in anh DMF (20 mL) was added K₂CO₃ (1.8 g, 12.9 mmol) in one portion. The mixture was heated at the reflux temp with stirring for 18 h and then allowed to cool to room temp. The mixture was then poured into water (100 mL) and extracted with EtOAc (3×100 mL). The combined organics were sequentially washed with water (3×50 mL) and a saturated NaCl solution (2×50 mL), dried (Na₂SO₄), and concentrated in vacuo to afford the desired product (0.8 g, 54%). The crude product was carried to the next step without further purification.

Step 2. 4-(3,4-Dimethoxyphenoxy)aniline: A solution of 4-(3,4-dimethoxy-phenoxy)-1-nitrobenzene (0.8 g, 3.2 mmol) in EtOAc (50 mL) was added to 10% Pd/C (0.100 g) and the resulting mixture was placed under a H₂ atmosphere (balloon) and was allowed to stir for 18 h at room temp. The mixture was then filtered through a pad of Celite® and concentrated in vacuo to afford the desired product as a white solid (0.6 g, 75%): EI-MS m/z 245 (M⁺).

A3f. General Method for Substituted Aniline Formation via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 3-(3-Pyridinyloxy)-1-nitrobenzene: To a solution of 3-hydroxypyridine (2.8 g, 29.0 mmol), 1-bromo-3-nitrobenzene (5.9 g, 29.0 mmol) and copper(I) bromide (5.0 g, 34.8 mmol) in anh DMF (50 mL) was added K₂CO₃ (8.0 g, 58.1 mmol) in one portion. The resulting mixture was heated at the reflux temp. with stirring for 18 h and then allowed to cool to room temp. The mixture was then poured into water (200 mL) and extracted with EtOAc (3×150 mL). The combined organics were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na₂SO₄), and concentrated in vacuo. The resulting oil was purified by flash chromatography (30% EtOAc/70% hexane) to afford the desired product (2.0 g, 32%). This material was used in the next step without further purification.

Step 2. 3-(3-Pyridinyloxy)aniline: A solution of 3-(3-pyridinyloxy)-1-nitrobenzene (2.0 A, 9.2 mmol) in EtOAc (100 mL) was added to 10% Pd/C (0.200 g) and the resulting mixture was placed under a H₂ atmosphere (balloon) and was allowed to stir for 18 h at room temp. The mixture was then filtered through a pad of Celite® and concentrated in vacuo to afford the desired product as a red oil (1.6 g, 94%): EI-MS m/z 186 (M⁺).

A3 g. General Method for Substituted Aniline Formation via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 3-(5-Methyl-3-pyridinyloxy)-1-nitrobenzene: To a solution of 3-hydroxy-5-methylpyridine (5.0 g, 45.8 mmol), 1-bromo-3-nitrobenzene (12.0 g, 59.6 mmol) and copper(I) iodide (10.0 g, 73.3 mmol) in anh DMF (50 mL) was added K₂CO₃ (13.0 g, 91.6 mmol) in one portion. The mixture was heated at the reflux temp. with stirring for 18 h and then allowed to cool to room temp. The mixture was then poured into water (200 mL) and extracted with EtOAc (3×150 mL). The combined organics were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na₂SO₄), and concentrated in vacuo. The resulting oil was purified by flash chromatography (30% EtOAc/70% hexane) to afford the desired product (1.2 g, 13%).

Step 2. 3-(5-Methyl-3-pyridinyloxy)-1-nitrobenzene: A solution of 3-(5-methyl-3-pyridinyloxy)-1-nitrobenzene (1.2 g, 5.2=mol) in EtOAc (50 mL) was added to 10% Pd/C (0.100 g) and the resulting mixture was placed under a H₂ atmosphere (balloon) and was allowed to stir for 18 h at room temp. The mixture was then filtered through a pad of Celite® and concentrated in vacuo to afford the desired product as a red oil (0.9 g, 86%): CI-MS m/z 201 ((M+H)⁺).

A3 h. General Method for Substituted Aniline Formation via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 5-Nitro-2-(4-methylphenoxy)pyridine: To a solution of 2-chloro-5-nitropyridine (6.34 g, 40 mmol) in DMF (200 mL) were added of 4-methylphenol (5.4 g, 50 mmol, 1.25 equiv) and K₂CO₃ (8.28 g, 60 mmol, 1.5 equiv). The mixture was stirred overnight at room temp. The resulting mixture was treated with water (600 mL) to generate a precipitate. This mixture was stirred for 1 h, and the solids were separated and sequentially washed with a 1 N NaOH solution (25 mL), water (25 mL) and pet ether (25 mL) to give the desired product (7.05 g, 76%); mp 80-82° C.; TLC (30% EtOAc/70% pet ether) R_(f) 0.79; ¹H-NMR (DMSO-d₆) δ 2.31 (s, 3H), 7.08 (d, f=8.46 Hz, 2H), 7.19 (d, J=19.20 Hz, 1H), 7.24 (d, J=8.09 Hz, 2H), 8.58 (dd, J=2.94, 8.82 Hz, 1H), 8.99 (d, J=2.95 Hz, 1H); FAB-MS m/z (rel abundance) 231 ((M+H)⁺), 100%).

Step 2. 5-Amino-2-(4-methylphenoxy)pyridine Dihydrochloride; A solution 5-nitro-2-(4-methylphenoxy)pyridine (6.94 g, 30 mmol, 1 eq) and EtOH (10 mL) in EtOAc (190 mL) was purged with argon then treated with 10% Pd/C (0.60 g). The reaction mixture was then placed under a H₂ atmosphere and was vigorously stirred for 2.5 h. The reaction mixture was filtered through a pad of Celite®. A solution of HCl in Et₂O was added to the filtrate was added dropwise. The resulting precipitate was separated and washed with EtOAc to give the desired product (7.56 g, 92%): mp 208-210° C. (dec); TLC (50% EtOAc/50% pet ether) R_(f) 0.42; ¹H-NMR (DMSO-d₆) δ 2.25 (s, 3H)_(,) 6.98 (d, J=8.45 Hz, 2H), 7.04 (d, J=8.82 Hz, 1H), 7.19 (d, J=8.09 Hz, 2H), 8.46 (dd, J=2.57, 8.46 Hz, 1H), 8.63 (d, J=2.57 Hz, 1H); EI-MS m/z (rel abundance) (M⁺, 100%).

A3i. General Method for Substituted Aniline Formation via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 4-(3-Thienylthio)-1-nitrobenzene; To a solution of 4-nitrothiophenol (80% pure, 1.2 g, 6.1 mmol), 3-bromothiophene (1.0 g, 6.1 mmol) and copper(II) oxide (0.5 g, 3.7 mmol) in anhydrous DMF (20 mL) was added KOH (0.3 g, 6.1 mmol), and the resulting mixture was heated at 130° C. with stirring for 42 h and then allowed to cool to room temp. The reaction mixture was then poured into a mixture of ice and a 6N HCl solution (200 mL) and the resulting aqueous mixture was extracted with EtOAc (3×100 mL). The combined organic layers were sequentially washed with a 1M NaOH solution (2×100 mL) and a saturated NaCl solution (2×100 mL), dried (MgSO₄), and concentrated in vacuo. The residual oil was purified by MPLC (silica gel; gradient from 10% EtOAc/90% hexane to 5% EtOAc/95% hexane) to afford of the desired product (0.5 g, 34%). GC-MS m/z 237 (M⁺).

Step 2. 4-(3-Thienylthio)aniline: 4-(3-Thienylthio)-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method A1.

A3j. General Method for Substituted Aniline Formation via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

4-(5-Pyrimininyloxy)aniline: 4-Aminophenol (1.0 g, 9.2 mmol) was dissolved in DMF (20 μL) then 5-bromopyrimidine (1.46 g, 9.2 mmol) and 1(2CO₃ (1.9 g, 13.7 mmol) were added. The mixture was heated to 100° C. for 18 h and at 130° C. for 48 h at which CC-MS analysis indicated some remaining starting material. The reaction mixture was cooled to room temp. and diluted with water (50 mL). The resulting solution was extracted with EtOAc (100 mL). The organic layer was washed with a saturated NaCl solution (2×50 mL), dried (MgSO₄), and concentrated in vacuo. The residual solids were purified by MPLC (50% EtOAc/50% hexanes) to give the desired amine (0.650 g, 38%).

A3k. General Method for Substituted Aniline Formation via Nitroarene Formation through Nucleophilic Aromatic Substitution, Followed by Reduction

Step 1. 5-Bromo-2-methoxypyridine: A mixture of 2,5-dibromopyridine (5.5 g, 23.2 mmol) and NaOMe (3.76 g, 69.6 mmol) in MeOH (60 mL) was heated at 70° C. in a sealed reaction vessel for 42 h, then allowed to cool to room temp. The reaction mixture was treated with water (50 mL) and extracted with EtOAc (2×100 mL). The combined organic layers were dried (Na₂SO₄) and concentrated under reduced pressure to give a pale yellow, volatile oil (4.1 g, 95% yield): TLC (10% EtOAc/90% hexane) R_(f) 0.57.

Step 2. 5-Hydroxy-2-methoxypyridine: To a stirred solution of 5-bromo-2-methoxypyridine (8.9 g, 47.9 mmol) in THF (175 mL) at −78° C. was added an n-butyllithium solution (2.5 M in hexane; 28.7 mL, 71.8 mmol) dropwise and the resulting mixture was allowed to stir at −78° C. for 45 min. Trimethyl borate (7.06 mL, 62.2 mmol) was added via syringe and the resulting mixture was stirred for an additional 2 h. The bright orange reaction mixture was warmed to 0° C. and was treated with a mixture of a 3 N NaOH solution (25 mL, 71.77 mmol) and a hydrogen peroxide solution (30%; approx. 50 mL). The resulting yellow and slightly turbid reaction mixture was warmed to room temp. for 30 min and then heated to the reflux temp. for 1 h. The reaction mixture was then allowed to cool to room temp. The aqueous layer was neutralized with a 1N HCl solution then extracted with Et₂O (2×100 mL). The combined organic layers were dried (Na₂SO₄) and concentrated under reduced pressure to give a viscous yellow oil (3.5 g, 60%).

Step 3. 4-(5-(2-Methoxy)pyridyl)oxy-1-nitrobenzene: To a stirred slurry of NaH (97%, 1.0 g, 42 mmol) in anh DMF (100 mL) was added a solution of 5-hydroxy-2-methoxypyridine (3.5 g, 28 mmol) in DMF (100 mL). The resulting mixture was allowed to stir at room temp. for 1 h, 4-fluoronitrobenzene (3 mL, 28 mmol) was added via syringe. The reaction mixture was heated to 95° C. overnight, then treated with water (25 mL) and extracted with EtOAc (2×75 mL). The organic layer was dried (MgSO₄) and concentrated under reduced pressure. The residual brown oil was crystallized EtOAc/hexane) to afford yellow crystals (5.23 g, 75%).

Step 4. 4-(5-(2-Methoxy)pyridyl)oxyaniline: 4-(5-(2-Methoxy)pyridyl)oxy-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method A3d, Step 2.

A4a. General Method for Substituted Aniline Synthesis via Nucleophilic Aromatic Substitution Using a Halopyridine

3-(4-Pyridinylthio)aniline: To a solution of 3-aminothiophenol (3.8 mL, 34 mmoles) in anh DMF (90 mL) was added 4-chloropyridine hydrochloride (5.4 g, 35.6 mmoles) followed by K₂CO₃ (16.7 g, 121 mmoles). The reaction mixture was stirred at room temp. for 1.5 h, then diluted with EtOAc (100 mL) and water (100 mL). The aqueous layer was back-extracted with EtOAc (2×100 mL). The combined organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO₄), and concentrated under reduced pressure. The residue was filtered through a pad of silica (gradient from 50% EtOAc/50% hexane to 70% EtOAc/30% hexane) and the resulting material was triturated with a Et₂O/hexane solution to afford the desired product (4.6 g, 66%): TLC (100% ethyl acetate) R_(f) 0.29; ¹H-NMR (DMSO-d₆) δ 5.41 (s, 2H), 6.64-6.74 (m, 3H), 7.01 (d, J=4.8, 2H), 7.14 (t, J=7.85 Hz, 1H), 8.32 (d, J=4.8, 2H).

A4b. General Method for Substituted Aniline Synthesis Via Nucleophilic Aromatic Substitution Using a Halopyridine

4-(2-Methyl-4-pyridinyloxy)aniline: To a solution of 4-aminophenol (3.6 g, 32.8 mmol) and 4-chloropicoline (5.0 g, 39.3 mmol) in art DMPU (50 mL) was added potassium tert butoxide (7.4 g, 65.6 mmol) in one portion. The reaction mixture was heated at 100° C. with stirring for 18 h, then was allowed to coot to room temp. The resulting mixture was poured into water (200 mL) and extracted with EtOAc (3×150 mL). The combined extracts were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na₂SO₄), and concentrated in vacuo. The resulting oil was purified by flash chromatography (50% EtOAc/50% hexane) to afford the desired product as a yellow oil (0.7 g, 9%): CI-MS m/z 201 ((M+H)⁺).

A4c. General Method for Substituted Aniline Synthesis Via Nucleophilic Aromatic Substitution Using a Halopyridine

Step 1. Methyl(4-nitrophenyl)-4-pyridylamine: To a suspension of N-methyl-4-nitroaniline (2.0 g, 13.2 mmol) and K₂CO₃ (7.2 g, 52.2 mmol) in DMPU (30 mL) was added 4-chloropyridine hydrochloride (2.36 g, 15.77 mmol). The reaction mixture was heated at 90° C. for 20 h, then cooled to room temperature. The resulting mixture was diluted with water (100 mL) and extracted with EtOAc (100 mL). The organic layer was washed with water (100 mL), dried (Na₂SO₄) and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, gradient from 80% EtOAc/20% hexanes to 100% EtOAc) to afford methyl(4-nitrophenyl)-4-pyridylamine (0.42 g)

Step 2. Methyl(4-aminophenyl)-4-pyridylamine: Methyl(4-nitrophenyl)-4-pyridylamine was reduced in a manner analogous to that described in Method A1.

A5. General Method of Substituted Aniline Synthesis Via Phenol Alkylation Followed by Reduction of a Nitroarene

Step 1. 4-(4-Butoxyphenyl)thio-1-nitrobenzene: To a solution of 4(4-nitrophenyl-thio)phenol (1.50 g, 6.07 mmol) in anh DMF (75 ml) at 0° C. was added NaH (60% in mineral oil, 0.267 g, 6.67 mmol). The brown suspension was stirred at 0° C. until gas evolution stopped (15 min), then a solution of iodobutane (1.12 g, 690 ml, 6.07 mmol) in anh DMF (20 mL) was added dropwise over 15 min at 0° C. The reaction was stirred at room temp. for 18 h at which time TLC indicated the presence of unreacted phenol, and additional iodobutane (56 mg, 9.035 mL, 0.303 mmol, 0.05 equiv) and NaH (13 mg, 0.334 mmol) were added. The reaction was stirred an additional 6 h at room temp., then was quenched by the addition of water (400 mL). The resulting mixture was extracted with Et₂O (2×500 mL). The combined organics were washed with water (2×400 mL), dried (MgSO₄), and concentrated under reduced pressure to give a clear yellow oil, which was purified by silica gel chromatography (gradient from 20% EtOAc/80% hexane to 50% EtOAc/50% hexane) to give the product as a yellow solid (1.24 g, 67%): TLC (20% EtOAc/80% hexane) R_(f) 0.75; ¹H-NMR (DMSO-d₆) δ 0.92 (t, J=7.5 Hz, 3H), 1.42 (app hex, J=7.5 Hz, 2H), 1.70 (m, 2H), 4.01 (t, 16.6 Hz, 2H), 7.08 (d J=8.7 Hz, 2H), 7.17 (d, J=9 Hz, 2H), 7.51 (d, J=8.7 Hz, 2H), 8.09 (d, J=9 Hz, 2H).

Step 2. 4-(4-Butoxyphenyl)thioaniline: 4-(4-Butoxyphenyl)thio-1-nitrobenzene was reduced to the aniline in a manner analagous to that used in the preparation of 3-(trifluoromethyl)-4-(4-pyridinylthio)aniline (Method A3b, Step 2): TLC (33% EtOAc/77% hexane) R_(f) 0.38.

A6. General Method for Synthesis of Substituted Anilines by the Acylation of Diaminoarenes

4-(4-tert-Butoxycarbamoylbenzyl)aniline: To a solution of 4,4′-methylenedianiline (3.00 g, 15.1 mmol) in anh THF (50 mL) at room temp was added a solution of di-tert-butyl dicarbonate (3.30 g, 15.1 mmol) in anh THF (10 mL). The reaction mixture was heated at the reflux temp. for 3 h, at which time TLC indicated the presence of unreacted methylenedianiline. Additional di-tert-butyl dicarbonate (0.664 g, 3.03 mmol, 0.02 equiv) was added and the reaction stirred at the reflux temp. for 16 h. The resulting mixture was diluted with Et₂O (200 mL), sequentially washed with a saturated NaHCO₃ solution (100 ml), water (100 mL) and a saturated NaCl solution (50 mL), dried (MgSO₄), and concentrated under reduced pressure. The resulting white solid was purified by silica gel chromatography (gradient from 33% EtOAc/67% hexane to 50% EtOAc/50% hexane) to afford the desired product as a white. solid (2.09 g, 46%); TLC (50% EtOAc/50% hexane) R_(f)0.45; ¹H-NMR (DMSO-d₆) δ 1.43 (s, 9H), 3.63 (s, 2H), 4.85 (br s, 2H), 6.44 (d, J=8.4 Hz, 2H), 6.80 (d, J=8.1 Hz, 2H), 7.00 (d, J=8.4 Hz, 2H), 7.28 (d, J=8.1 Hz, 2H), 9.18 (hr s, 1H); FAB-MS m/z 298 (M⁺).

A7. General Method for the Synthesis of Aryl Amines Via Electrophilic Nitration Followed by Reduction

Step 1. 3-(4-Nitrobenzyl)pyridine: A solution of 3-benzylpyridine (4.0 g, 23.6 mmol) and 70% nitric acid (30 mL) was heated overnight at 50° C. The resulting mixture was allowed to cool to room temp. then poured into ice water (350 mL). The aqueous mixture then made basic with a 1N NaOH solution, then extracted with Et₂O (4×100 mL). The combined extracts were sequentially washed with water (3×100 mL) and a saturated NaCl solution (2×100 mL), dried (Na₂SO₄), and concentrated in vacuo. The residual oil was purified by MPLC (silica gel; 50% EtOAc/50% hexane) then recrystallization (EtOAc/hexane) to afford the desired product (1.0 g, 22%): CC-MS m/z 214 (M⁺).

Step 2. 3-(4-Pyridinyl)methylaniline: 3-(4-Nitrobenzyl)pyridine was reduced to the aniline in a manner analogous to that described in Method A1.

A8. General Method for Synthesis of Aryl Amines Via Substitution with Nitrobenzyl Halides Followed by Reduction

Step 1. 4-(1-Imidazolylmethyl)-1-nitrobenzene: To a solution of imidazole (0.5 g, 7.3 mmol) and 4-nitrobenzyl bromide (1.6 g, 7.3 mmol) in anh acetonitrile (30 mL) was added K₂CO₃ (1.0 g, 7.3 mmol). The resulting mixture was stirred at room temp. for 18 h and then poured into water (200 mL) and the resulting aqueous solution was extracted with EtOAc (3×50 mL). The combined organic layers were sequentially washed with water (3×50 mL) and a saturated NaCl solution (2×50 mL), dried (MgSO₄), and concentrated in vacuo. The residual oil was purified by MPLC (silica gel; 25% EtOAc/75% hexane) to afford the desired product (1.0 g, 91%): EI-MS m/z 203 (M⁺).

Step 2. 4-(1-Imidazolylmethyl)aniline: 4-(1-Imidazolylmethyl)-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method A2.

A9. Formation of Substituted Hydroxymethylanilines by Oxidation of Nitrobenzyl Compounds Followed by Reduction

Step 1. 4-(1-Hydroxy-1-(4-pyridyl)methyl-1-nitrobenzene: To a stirred solution of 3-(4-nitrobenzyl)pyridine (6.0 g, 28 mmol) in CH₂Cl₂ (90 mL) was added m-CPBA (5.80 g, 33.6 mmol) at 10° C., and the mixture was stirred at room temp. overnight. The reaction mixture was successively washed with a 10% NaHSO₃ solution (50 mL), a saturated K₂CO₃ solution (50 mL) and a saturated NaCl solution (50 mL), dried (MgSO₄) and concentrated under reduced pressure. The resulting yellow solid (2.68 g) was dissolved in anh acetic anhydride (30 mL) and heated at the reflux temperature overnight. The mixture was concentrated under reduced pressure. The residue was dissolved in MeOH (25 mL) and treated with a 20% aqueous NH₃ solution (30 mL). The mixture was stirred at room temp. for 1 h, then was concentrated under reduced pressure. The residue was poured into a mixture of water (50 mL) and CH₂Cl₂ (50 mL). The organic layer was dried (MgSO₄), concentrated under reduced pressure, and purified by column chromatography (80% EtOAc/20% hexane) to afford the desired product as a white solid. (0.53 g, 8%); mp 110-118° C.; TLC (80% EtOAc/20% hexane) R_(f) 0.12; FAB-MS m/z 367 ((M+H)⁺, 100%).

Step 2. 4-(1-Hydroxy-1-(4-pyridyl)methylaniline: 4-(1-Hydroxy-1-(4-pyridyl)-methyl-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method A3d, Step 2.

A10. Formation of 2-(N-methylcarbamoyl)pyridines Via the Menisci reaction

Step 1. 2-(N-methylcarbamoyl)-4-chloropyridine. (Caution: this is a highly hazardous, potentially explosive reaction.) To a solution of 4-chloropyridine (10.0 g) in N-methylformamide (250 mL) under argon at ambient temp was added conc. H₂SO₄ (3.55 mL) (exotherm). To this was added H₂O₂ (17 mL, 30% wt in H2O) followed by FeSO₄7H₂O (0.55 g) to produce an exotherm. The reaction was stirred in the dark at ambient temp for 1 h then was heated slowly over 4 h at 45° C. When bubbling subsided, the reaction was heated at 60° C. for 16 h. The opaque brown solution was diluted with H2O (700 mL) followed by a 10% NaOH solution (250 mL). The aqueous mixture was extracted with EtOAc (3×500 ml) and the organic layers were washed separately with a saturated NaCl solution (3×150 mL. The combined organics were dried (MgSO₄) and filtered through a pad of silica gel eluting with EtOAc. The solvent was removed in vacuo and the brown residue was purified by silica gel chromatography (gradient from 50% EtOAc/50% hexane to 80% EtOAc/20% hexane). The resulting, yellow oil crystallized at 0° C. over 72 h to give 2-(N-methylcarbamoyl)-4-chloropyridine in yield (0.61 g, 5.3%): TLC (50% EtOAc/50% hexane) R_(f) 0.50; MS; ¹H NMR (CDCl₃): δd 8.44 (d, 1H, J=5.1 Hz, CNN), 8.21 (s, 1H, CHCCO), 7.96 bs, 5H, NH), 7.43 (dd, 1H, J=2.4, 5.4 Hz, ClCHCN), 3.04 (d, 3H, J=5.1 Hz, methyl); CI-MS m/z 171 ((M+H)+).

A11. General Method for the Synthesis of δ-Sulfonylphenyl Anilines

Step 1. 4-(4-Methylsulfonylphenoxy)-1-nitrobenzene: To a solution of 4-(4-methylthiophenoxy)-1-nitrobenzene (2 g, 7.66 mmol) in CH₂Cl₂ (75 mL) at 0° C. was slowly added mCPBA (57-86%, 4 g), and the reaction mixture was stirred at room temperature for 5 h. The reaction mixture was treated with a 1 N NaOH solution (25 mL). The organic layer was sequentially washed with a 1N NaOH solution (25 mL), water (25 mL) and a saturated NaCl solution (25 mL), dried (MgSO₄), and concentrated under reduced pressure to give 4-(4-methylsulfonylphenoxy)-1-nitrobenzene as a solid (2.1 g).

Step 2. 4-(4-Methylsulfonylphenoxy)-1-aniline: 4-(4-Methylsulfonylphenoxy)-1-nitrobenzene was reduced to the aniline in a manner analogous to that described in Method A3d, step 2.

A12. General Method for Synthesis of δ-Alkoxy-δ-carboxyphenyl Anilines

Step 1. 4-(3-Methoxycarbonyl-4-methoxyphenoxy)-1-nitrobenzene: To a solution of δ-(3-carboxy-4-hydroxyphenoxy)-1-nitrobenzene (prepared in a manner analogous to that described in Method A3a, step 1, 12 mmol) in acetone (50 mL) was added K₂CO₃ (5 g) and dimethyl sulfate (3.5 mL). The resulting mixture was heated at the reflux temperature overnight, then cooled to room temperature and filtered through a pad of Celite®. The resulting solution was concentrated under reduced pressure, absorbed onto silica gel, and purified by column chromatography (50% EtOAc/50% hexane) to give 4-(3-methoxycarbonyl-4-methoxyphenoxy)-1-nitrobenzene as a yellow powder (3 g): mp 115-118° C.

Step 2. 4-(3-Carboxy-4-methoxyphenoxy)-1-nitrobenzene: A mixture of 4-(3-methoxycarbonyl-4-methoxyphenoxy)-1-nitrobenzene (1.2 g), KOH (0.33 g), and water (5 mL) in MeOH (45 mL) was stirred at room temperature overnight and then heated at the reflux temperature for 4 h. The resulting mixture was cooled to room temperature and concentrated under reduced pressure. The residue was dissolved in water (50 mL), and the aqueous mixture was made acidic with a 1N HCl solution. The resulting mixture was extracted with EtOAc (50 mL). The organic layer was dried (MgSO₄) and concentrated under reduced pressure to give 4-(3-carboxy-4-methoxyphenoxy)-1-nitrobenzene (1.04 g).

B. General Methods of Urea Formation

B1. Reaction of a Heterocyclic Amine with an Aryl Isocyanate

N-(4-tert-butylpyridyl)-N′-(2,3-dichlorophenyl)urea: A solution of 2-amino-4-tert-butylpyridine (192 mg) and 2,3-dichlorophenyl isocyanate (240 mg) in anh. toluene (15 mL) was heated at 70° C. under argon for 24 h. The resulting mixture was diluted with EtOAc (200 mL) then washed with water (125 mL). The organic layer was dried (MgSO₄) and concentrated tinder reduced pressure to give a gum. Trituration of the gum with hexanes afforded N-(4-tert-butylpyridyl)-N′-(2,3-dichlorophenyl)urea as a white solid (394 mg, 91%): TLC (2:1 hexanes/ethyl acetate) R_(f) 0.40; FAB-MS m/z 338 ((M+H)⁺).

B2a. Reaction of a Heterocyclic Amine with N,N′-Carbonyldiimidazole Followed by Reaction with a Substituted Aniline

N-(4-tert-butylpyridyl)-N′-(4-(4-pyridinylmethyl)phenyl urea: To a stirring solution of 4-tert-butyl-2-aminopyridine (192 mg) in anh. CH₂Cl₂ (15 mL) under argon at 0° C. was added CDI (207 mg). The resulting solution was allowed to warm to ambient temp over 2 h. To this mixture was added 4-(4-pyridylmethyl)aniline (prepared according to Method A1, 235 mg). The resulting solution was stirred at room temperature for 24 h, then was quenched with water (125 ml). The resulting mixture was extracted with EtOAc (200 mL). The organic layer was washed with water (100 mL), dried (MgSO₄) and concentrated under reduced pressure. The residue was purified by chromatography (SiO₂, EtOAc) to afford N-(4-tert-butylpyridyl)-N′-(4-(4-pyridinylmethyl)phenyl urea as a white solid (200 mg, 43%): TLC (EtoAc) R_(f) 0.47; FAB-MS m/z 361 ((M+H)⁺).

B2b. Reaction of a Heterocyclic Amine with N,N′-Carbonyldiimidazole Followed by Reaction with a Substituted Aniline

N,N′-(Bis(3-(2-methoxyquinolinyl)) urea): To a stirring solution of: 3-amino-2-methoxyquinoline (133 mg) in anh. CH₂Cl₂ (15 mL) under argon at 0° C. was added CDI (128 mg). The resulting solution was warmed to ambient temp over 1 h. After 16 h 4-(2-N-Methylcarbamyl-4-pyridyloxy)aniline (175 mg) was added and the resulting yellow solution was stirred at room temperature under argon for 72 h. The solution was treated with water (125 mL) and the resulting mixture was extracted with EtOAc (2×150 mL). The combined organics were washed with a saturated NaCl solution (100 mL), dried (MgSO₄) and concentrated under reduced pressure. The residue was triturated with a 10% hexane/90% EtOAc solution. The resulting white crystals were washed with EtOAc. The resulting filtrate was purified by chromatography (SiO₂, 50% EtOAc/50% hexane) to give N,N′-(bis(3-(2-methoxyquinolinyl)) urea) (30 mg, 20% yield): TLC (50% EtOAc/50% hexane) R_(f) 0.45; HPLC ES-MS m/z 375 ((M+H)⁺).

B2c. Reaction of a Heterocyclic Amine with N,N-Carbonyldiimidazole Followed by Reaction with a Substituted Aniline

N-(4-tert-Butylpyridyl)-N′-(4-(4-chlorophenoxy)phenyl)urea: A solution of 4-tert-butyl-2-aminopyridine (0.177 g, 1.18 mmol, 1 equiv.) in 1.2 mL of anh. CH₂Cl₂ (1.2 mL) was added to CDI (0.200 g, 1.24 mmol, 1.05 equiv) and the mixture was allowed to stir under argon at room temperature 1d. To the resulting solution was added 4-(4-chlorophenoxy)aniline (0.259 g, 1.18 mmol, 1 equiv.) in one portion. The resulting mixture was stirred at room temperature for 1d, then was treated with a 10% citric acid solution (2 mL) and allowed to stir for 1 h. The resulting organic layer was extracted with EtOAc (3×5 mL). The combined organic layers were dried (MgSO₄) and concentrated in vacuo. The resultant residue was treated with CH₂Cl₂ (10 mL) and a 1 N aqueous NaOH solution. This mixture was allowed to stir overnight. The resulting organic layer was extracted with CH₂Cl₂ (3×5 mL). The combined organic layers were (MgSO₄) and concentrated in vacuo. The resultant solids were suspended in diethyl ether (10 mL) and sonicated for 15 minutes. The resulting white solids were dried to give N-(4-tert-butylpyridyl)-N′-(4-(4-chlorophenoxy)phenyl)urea (42 mg, 9%): mp 198-199° C.

B3. Reaction of Substituted Aniline with N,N′-Carbonyldiimidazole Followed by Reaction with a Heterocyclic Amine

N-(2-(5-trifluoromethyl)pyridyloxy)-N′-(3-(4-pyridylthio)phenyl)urea: A solution of 3-(4-pyridylthio)aniline (300 mg, 1.48 mmoles) in CH₂Cl₂ (12 mL) was treated with CDI (253 mg, 1.56 mmoles). The solution was stirred at room temperature and under argon for 2 h. The resulting mixture was treated with 2-amino-5-(trifluoromethyl)pyridine (238 mg, 1.47 mmoles) and heated at 40° C. overnight. The reaction mixture was then diluted with EtOAc (25 mL), washed with water (10 mL) and a saturated NaCl solution m(25 mL), dried (MgSO₄), and concentrated under reduced pressure. The residue was purified by column chromatography (SiO₂; gradient from 70% EtOAc/30% CH₂Cl₂ to 100% EtOAc to give N-(2-(5-trifluoromethyl)pyridyloxy)-N′-(3-(4-pyridylthio)phenyl)urea (103 mg): TLC (50% EtOAc/50% CH₂Cl₂) R_(f) 0.33; ¹H-NMR (DMSO-d₆) δ 6.06 (d, J=6 Hz, 2H), 7.25 (dt, J=1.2, 7.8 Hz, 1H), 7.48 (t, J=8.1 Hz, 1H), 7.59-7.63 (m, 1H), 7.77 (d, J=8.7 Hz, 1H), 7.86 (t, J=1.8 Hz, 1H), 8.12 (dd, J=2.7, 9.3 Hz, 1H), 8.37 (d, J=6.3 Hz, 2H), 8.67 (bs, 1H), 9.88 (s, 1H), 10.26 (s, 1H); FAB-MS m/z 391 ((M+H)⁺).

B4. Reaction of a Heterocyclic Amine with Phosgene, Followed by Reaction with a Substituted Aniline

N-(3-(2-methoxyquinolinyl)-N′-(4-(4-(2-N-Methylcarbamyl-4-pyridyloxy)phenyl) urea: To a stirring solution of phosgene (20% in toluene, 1.38 mL) in anh. CH₂Cl₂ (20 ml) at 0° C. under argon was added anh. pyridine (207 mg) followed by 3-amino-2-methoxyquinoline (456 mg). The resulting solution was warned to ambient temperature over 1 h, then concentrated in vacuo at ambient temperature to give a white solid. The solid was dried under vacuum for 15 min then suspended in art toluene (20 mL). To the resulting slurry was added 4-(4-(2-(methylcarbamoyl)pyridyloxy)aniline (prepared according to Method A2, 300 mg) and the reaction heated under argon at 80° C. for 20 h. The resulting mixture was diluted with water (200 mL), then treated with a saturated NaHCO₃ solution (10 mL) and extracted with EtOAc (2×300 mL). The combined organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO₄) and concentrated under reduced pressure. The solid yellow residue was purified by chromatography (SiO₂, gradient from 50% EtOAc/50% hexane 100% EtOAc), followed by recrystallization from diethyl ether and hexane to give N-(3-(2-methoxyquinolinyl)-N′-(4-(4-(2-N-Methylcarbamyl-4-pyridyloxy)phenyl)urea as a white solid (140 mg, 25%): TLC (EtOAc) R_(f) 0.52; FAB-MS m/z 430 ((M⁺+H)⁺),

Specific Compound Preparations

Descriptions of the detailed preparative steps used to prepare the specific compounds listed in Tables 1-4 are provided below. Many of the compounds listed in the Tables can be synthesized following a variety of methods. The specific examples below are therefore provided by way of illustration only and should not be construed to limit the scope of the invention in any way.

Entry 5: N-(4-tert-Butylpyridyl)-N′-(4-(4-pyridinylmethyl)phenyl urea was prepared according to Method B2a. Entry 6: 4-tert-Butyl-2-aminopyridine was reacted with 4-phenoxyaniline according to Method B2c to afford the urea. Entry 7: 4-tert-Butyl-2-aminopyridine was reacted with 4-(4-methylphenoxy)aniline according to Method B2c to afford the urea, Entry 8: N-(4-tert-Butylpyridyl)-N′-(4-(4-chlorophenoxy)phenyl)urea was prepared according to Method B2c. Entry 10: 4-(4-Aminophenoxy)pyridine was prepared starting from 4-hydroxypyridine and 1-bromo-3-nitrobenzene according to Method A3F. 4-tert-Butyl-2-aminopyridine was reacted with 4-(4-aminophenoxy)pyridine according to Method B2a to afford the urea. Entry 11: 4-(4-Pyridylthio)amine was prepared starting from 4-aminothiophenol and 4-chloropyridine hydrochloride according to Method A4a. 4-tert-Butyl-2-aminopyridine was reacted with 4-(4-pyridylthio)aniline according to Method B2c to afford the urea. Entry 12: 4-(4-Pyridylthio)aniline was prepared starting from 4-aminothiophenol and 4-chloropyridine hydrochloride according to Method A4a. 4-tert-Butyl-2-aminopyridine was reacted with 3-(4-pyridylthio)aniline according to Method B2c to afford the urea. Entry 20: 4-(4-Aminophenoxy)pyridine was prepared starting from 4-hydroxypyridine and 1-bromo-3-nitrobenzene according to Method A3f. 3-Aminoisoquinoline was reacted with 4-(4-aminophenoxy)pyridine according to Method B2a to afford the urea. Entry 22: N,N′-(Bis(3-(2-methoxyquinolinyl)) urea) was prepared according to Method B2b. Entry 23: 3-Amino-2-methoxyquinoline and 4-(4-pyridylmethyl)aniline were reacted according to Method B3 to afford the urea. Entry 24: 3-Amino-2-methoxyquinoline was reacted with 4-(4-pyridylcarbonyl)aniline according to Method B4 to afford the urea. Entry 25: 4-(4-Pyridyloxy)aniline was prepared starting from 4-hydroxypyridine and 1-fluoro-4-nitrobenzene according to Method A3d. 3-Amino-2-methoxyquinoline was reacted with 4-(4-pyridyloxy)aniline according to Method B2c to afford the urea. Entry 26: 3-Amino-2-methoxyquinoline was reacted with 4-((4 methoxyphenyl)methylamino)aniline according to Method B4 to afford the urea. Entry 27: 3-(4-Pyridylthio)aniline was prepared according to Method A4a. 3-Amino-2-methoxyquinoline and 3-(4-pyridylmethyl)aniline were reacted according to Method B3 to afford the urea. Entry 28: 4-(4-Pyridyloxy)aniline was prepared starting from 4-hydroxypyridine and 1-fluoro-4-nitrobenzene according to Method A3d. 1-(4-Methylpiperazinyl)-3-aminoisoquinoline was reacted with 4-(4-aminophenoxy)pyridine according to Method 82a to afford the urea.

The following compounds have been synthesized according to the General Methods listed above:

TABLE 1 4-tert-Butyl-2-pyridyl Ureas

TLC Mass mp HPLC TL Solvent Spec. Entry R (° C.) (min.) C R_(f) System [Source] 5

0.47 100%EtOAc 361(M + H) +(FAB) 6

179-180 0.58 5%MeOH/95%CH2Cl2 362(M + H) +(FAB) 7

190-191 0.46 5%MeOH/95%CH2Cl2 376(M + H) +(FAB) 8

198-199 0.76 5%MeOH/95%CH2Cl2 396(M + H) +(FAB) 10

0.40 100%EtOAc 363(M + H) +(FAB) 11

208-212 0.39 5%MeOH/95%CH2Cl2 379(M + H) +(HPLCES-MS) 12

196-197 0.37 5%MeOH/95%CH2Cl2 379(M + H) +(FAB)

TABLE 2 3-Isoquinolyl Ureas

TLC Mass mp HPLC TL Solvent Spec. Entry R (° C.) (min.) C R_(f) System [Source] 20

0.27 100%EtOAc 357(M + H) +(FAB)

TABLE 3 2-Methoxy-3-quinolyl Ureas

TLC Mass mp HPLC TL Solvent Spec. Entry R (° C.) (min.) C R_(f) System [Source] 22

0.45 50%EtOAc/50%hexane 375(M + H) +(HPLCES-MS) 23

0.56 50%EtOAc/50%hexane 385(M + H) +(FAB) 24

0.45 100%EtOAc 399(M + H) +(FAB) 25

207-208 0.24 5%MeOH/95%CH2Cl2 387(M + H) +(FAB) 26

126-130 27

0.39 50%acetone/50%CH2Cl2 403(M + H) +(FAB)

TABLE 4 3-Quinolyl Ureas

TLC Mass mp HPLC TL Solvent Spec. Entry R (° C.) (min.) C R_(f) System [Source] 28

0.20 30%MeOH/70%EtOAc 455(M + H) +(HPLCES-MS)

Biological Examples In Vitro raf Kinase Assay

In an in vitro kinase assay, raf was incubated with MEK in 20 mM Tris-HCl, pH 8.2 containing 2 mM 2-mercaptoethanol and 100 mM NaCl. This protein solution (20 μL) was mixed with water (5 μL) or with compounds diluted with distilled water from 10 mM stock solutions of compounds dissolved in DMSO. The kinase reaction was initiated by adding 25 μL [λ-³³P]ATP (1000-3000 dpm/pmol) in 80 mM Tris-HCl, pH 7.5, 120 mM NaCl, 1.6 mM DTT, 16 mM MgCl₂. The reaction-mixtures were incubated at 32° C., usually for 22 min. Incorporation of ³³P into protein was assayed by harvesting the reaction onto phosphocellulose mats, washing away free counts with a 1% phosphoric acid solution and quantitating phosphorylation by liquid scintillation counting. For high throughput screening, 10 μM ATP and 0.4 μM MEK was used. In some experiments, the kinase reaction was stopped by adding an equal amount of Laemmli sample buffer. Samples were boiled 3 min and the proteins resolved by electrophoresis on 7.5% Laemmli gels. Gels were fixed, dried and exposed to an imaging plate (Fuji). Phosphorylation was analyzed using a Fujix Bio-Imaging Analyzer System.

All compounds exemplified displayed IC₅₀s of between 10 nM and 10 μM.

Cellular Assay:

For in vitro growth assay, human tumor cell lines, including but not limited to HCT116 and DLD-1, containing mutated K-ras genes were used in standard proliferation assays for anchorage dependent growth on plastic or anchorage independent growth in soft agar. Human tumor cell lines were obtained from ATCC (Rockville M) and maintained in RPMI with 10% heat inactivated fetal bovine serum and 200 mM glutamine. Cell culture media and additives were obtained from Gibco/BRL (Gaithersburg, Md.) except for fetal bovine serum (JR Biosciences, Lenexa, Kans.). In a standard proliferation assay for anchorage dependent growth, 3×10³ cells were seeded into 96-well tissue culture plates and allowed to attach overnight at 37° C. in a 5% CO₂ incubator. Compounds were titrated in media in dilution series and added to 96-well cell cultures. Cells were allowed to grow 5 days typically with a feeding of fresh compound containing media on day three Proliferation was monitored by measuring metabolic activity with standard XTT colorimetric assay (Boehringer Mannheim) measured by standard ELISA plate reader at OD 490/560, or by measuring ³H-thymidine incorporation into DNA following an 8 h culture with 1 μCu ³H-thymidine, harvesting the cells onto glass fiber mats using a cell harvester and measuring-³H-thymidine incorporation by liquid scintillant counting.

For anchorage independent cell growth, cells were plated at 1×10³ to 3×10³ in 0.4% Seaplaque agarose in RPMI complete media, overlaying a bottom layer containing only 0.64% agar in PRMI complete media in 24-well tissue culture plates. Complete media plus dilution series of compounds were added to wells and incubated at 37° C. in a 5% CO₂ incubator for 10-14 days with repeated feedings of fresh media containing compound at 3-4 day intervals. Colony formation was monitored and total cell mass, average colony size and number of colonies were quantitated using image capture technology and image analysis software (Image Pro Plus, media Cybernetics).

These assays established that the compounds of formula I are active to inhibit raf kinase activity and to inhibit oncogenic cell growth.

In Vivo Assay;

An in vivo assay of the inhibitory effect of the compounds on tumors (e.g., solid cancers) mediated by raf kinase can be performed as follows;

CDI nu/nu mice (6-8 weeks old) are injected subcutaneously into the flank at 1×10⁶ cells with human colon adenocarcinoma cell line. The mice are dosed i.p., i.v. or p.o. at 10, 30, 100, or 300 mg/Kg beginning on approximately day 10, when tumor size is between 50-100 mg. Animals are dosed for 14 consecutive days once a day; rumor size was monitored with calipers twice a week.

The inhibitory effect of the compounds on raf kinase and therefore on tumors (e.g., solid cancers) mediated by raf kinase can further be demonstrated in vivo according to the technique of Monia et al. (Nat. Med. 1996, 2, 668-75).

The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.

From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention and, without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions. 

1-20. (canceled)
 21. A method for inhibiting raf kinase in a patient, comprising administering an effective amount of a compound of one of the following formulae A-D-B  (I) A′-D-B′  (II) and A″-D-B″  (III) or a pharmaceutically acceptable salt thereof, wherein D is —NH—C(O)—NH—, A is selected from the group consisting of substituted t-butylpyridyl groups, unsubstituted t-butylpyridyl groups, substituted (trifluoromethyl)pyridyl groups, unsubstituted (trifluoromethyl) pyridyl groups, substituted isopropylpyridyl groups, unsubstituted isoproplpyridyl groups, substituted (2-methyl-2-butyl)pyridyl groups, unsubstituted (2-methyl-2-butyl pyridyl) groups, substituted (3-methyl-3-pentyl)pyridyl groups, and unsubstituted (3-methyl-3-pentyl)pyridyl groups, substituted (3-ethyl-3-pentyl)pyridyl groups and unsubstituted (3-ethyl-3-pentyl)pyridyl groups A′ is a substituted isoquinolinyl group or unsubstituted isoquinolinyl group or an unsubstituted quinolinyl group, A″ is a substituted quinolinyl group, B, B′ and B″ are each, independently, a substituted or unsubstituted bridged cyclic structure of up to 30 carbon atoms of the formula -L-(ML¹)_(q) wherein L comprises a cyclic moiety having at least 5 members and is bound directly to D, L¹ comprises a cyclic moiety having at least 5 members, M is a bridging group selected from the group consisting of —O—, —S—, —N(R⁷)—, —(CH—)_(m)—, —C(O)—, —CH(OH)—, —(CH₂)_(m)O—, —(CH₂)_(m)S—, —(CH₂)_(m)N(R⁷)—, —O(CH₂)_(m), CHX^(a)—, —CX^(a) ₂—, —S—(CH₂)_(m)— and —N(R⁷)(CH₂)_(m)—, where m=1-3 X^(a) is halogen, and R⁷ is as defined below, q is an integer of from 1-3, and each cyclic structure of L and L¹ contains 0-4 members of the group consisting of nitrogen, oxygen and sulfur, subject to the provisos that B is not

and B″ is not

wherein the substituents for A″ and the substituted isoquinolyl groups of A′ are selected from the group consisting of halogen, up to per-halo, and Wn, where n is 0-3 and each W is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, at least a five membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O; —CN, up to per halo substituted C₆-C₁₄ aryl, up to per halo substituted C₇-C₂₄ alkaryl, up to per halo substituted C₇₋₄ aralkyl, up to per halo substituted C₃-C₁₂ heteroaryl having at least 5 members and 1-3 heteratoms selected from O, N and S, up to per halo substituted C₄-C₂₄ alkylheteroaryl having at least 5 members and 1-3 heteroatoms selected from O, N and S, C₆-C₁₄ aryl, C₁-C₂₄ alkaryl, C₁-C₂₄ aralkyl, C₃-C₁₂ heteroaryl having at least 5 cyclic members and 1-3 heteroatoms selected from O, N and S, C₄-C₂₄ alkylheteroaryl having at least 5 cyclic members and 1-3 heteroatoms selected from O, N and S; —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ alkenyl and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein the substitutents for the substituted t-butyl pyridyl groups substituted trifluoromethyl pyridyl groups, substituted isopropyl pyridyl groups, substituted 2-methyl-2-butyl pyridyl groups and substituted 3-methyl-3-pentyl pyridyl groups of A are selected from the group consisting of halogen, up to per-halo, and Zn, where n is 0-3 and each Z is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W; where B and B′ are substituted, the substituents are selected from the group consisting of halogen, up to per-halo, and Jn, where n is 0-3 and each J is independently selected from the group consisting of —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, at least a five-membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, C₆₋₁₂ aryl, at least a five-membered C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, C₇₋₂₄ aralkyl, C₇₋₂₄ alkaryl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O, substituted C₆-C₁₄ aryl, at least a five-membered substituted C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, substituted C₇₋₂₄ alkaryl and substituted C₇-C₂₄ aralkyl, where B″ is substituted, the substituents are selected from the group consisting of halogen, —CN, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7″) independently as defined above for W, C₁₋₁₀ alkyl, at least a five-membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, C₆₋₁₂ aryl, at least a five-membered C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, C₇₋₄ aralkyl, C₇₋₂₄ alkaryl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O, substituted C₆-C₁₄ aryl, at least a five-membered substituted C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, substituted C₇₋₂₄ alkaryl and substituted C₇-C₂₄ aralkyl, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), —C(O)NR^(a)R^(b) and —SO₂R^(a) wherein each R^(a) and R^(b) are independently hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O, where J is a substituted group, it is substituted by halogen, up to per halo, or by one or more substituents independently selected from the group consisting of —CN, —CO₂R⁷, —OR⁷, —SR⁷, —NR⁷R^(7′), —NO₂, —NR⁷C(O)R^(7′) and —NR⁷C(O)OR^(7′); with each R⁷ and R^(7′) independently as defined above for W, a patient in need thereof.
 22. A method as in claim 21 for inhibiting raf kinase in a patient, comprising administering an effective amount of a compound of one of the following formulae A-D-B, A′-D-B′, A″-D-B″,

R is selected from the group consisting of halogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), or a pharmaceutically acceptable salt thereof wherein D is —NH—C(O)—NH— A is selected from the group consisting of substituted t-butylpyridyl groups, unsubstituted t-butylpyridyl group, substituted (trifluoromethyl)pyridyl group, unsubstituted (trifluoromethyl) pyridyl group, substituted isopropylpyridyl group, unsubstituted isopropylpyridyl group, substituted (2-methyl-2-butyl)pyridyl group, unsubstituted (2-methyl-2-butyl) pyridyl group, substituted (3-methyl-3-pentyl) pyridyl group, unsubstituted (3-methyl-3-pentyl) pyridyl group, substituted (3-ethyl-3-pentyl)pyridyl group, unsubstituted (3-ethyl-3-pentyl) pyridyl group, A′ is a substituted isoquinolinyl group or unsubstituted isoquinolinyl group or an unsubstituted quinolinyl group, A″ is a substituted quinolinyl group, B, B′ and B″ are each independently of the formula -L-(ML¹)_(q), wherein L is phenyl or substituted phenyl and L¹ is phenyl, substituted phenyl, pyridinyl or substituted pyridinyl, q is an integer of from 1-2 and M is selected from the group consisting of —O—, —S—, —N(R⁷)—, —(CH₂)_(m)—, —C(O)—, —CH(OH)—, —(CH₂)_(m)O—, —(CH₂)_(m)S—, —(CH₂)_(m)N(R⁷)—, —O(CH₂)_(m), CHX^(a)—, CX^(a) ₂—, —S—(CH₂)— and —N(R⁷)(CH₂)_(m)—, where m=1-3, X^(a) is halogen, and R⁷ is as defined below; subject to the provisos that B′ is not

B is not

wherein the substituents for the substituted t-butyl pyridyl groups, substituted trifluoromethyl pyridyl groups, substituted isopropyl pyridyl groups, substituted 2-methylbutyl pyridyl groups and 3-methylpentyl pyridyl groups, of A are selected from the group consisting of halogen, up to per-halo, and Zn, where n is 0-3 and each Z is independently selected from the group consisting of C₁₋₁₀ alkyl C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein the substituents for A″ and the substituted isoquinolinyl groups of A′ are selected from the group consisting of halogen, up to per-halo, and Wn, where n is 0-3 and each W is independently selected from the group consisting. of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ alkenyl and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein B and B′ are substituted, the substituents are selected from the group consisting of halogen, up to per-halo, and Jn, where n is 0-3 and each J is independently selected from the group consisting of —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, and substituted C₁₋₁₀ alkoxy, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), —C(O)NR^(a)R^(b) and —SO₂R^(a) wherein R^(a) and R^(b) are each independently hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O, wherein B″ is substituted, the substituents are selected from the group consisting of halogen, —CN, —C(O)NR⁷R^(7′), —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, and substituted C₁₋₁₀ alkoxy, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), C(O)NR^(a)R^(b) and —SO₂R^(a) wherein R^(a) and R^(b) are each independently, hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O to a patient in need thereof.
 23. A method as in claim 21 for inhibiting raf kinase in a patient, comprising administering an effective amount of a compound which is N-(4-tert-butylpyridinyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-phenoxyphenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-methylphenoxy)phenyl) or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-chlorophenoxy)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-pyridinyloxy)phenyl)urea or a pharmaceutically acceptable salt thereof; N-4-tert-butylpyridinyl)-N′-(4-(4-pyridinylthio)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-3-(4-pyridinylthio)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(3-isoquinolinyl)-N′-(4-(4-pyridinyloxy)phenyl)urea or a pharmaceutically acceptable salt thereof; N,N′-(bis(3-(2-methoxyquinolinyl)) urea) or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinylmethyl)phenyl)) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinylcarbonyl)phenyl)) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinyloxy)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-methoxyphenyl)methylamino)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(3-(4-pyridinylthio)phenyl))urea or a pharmaceutically acceptable salt thereof; or N-(1-(4-methylpiperazinyl)-3-isoquinolinyl)-N′ (4-(4-pyridinyloxy)phenyl)urea or a pharmaceutically acceptable salt thereof to a patient in need thereof. 24-40. (canceled)
 41. A method for treating a solid tumor with cell growth mediated by raf kinase in a patient, comprising administering a therapeutically effective amount of a compound of one of the following formulae A-D-B  (I) A′-D-B′  (II) and A″-D-B″  (III) or a pharmaceutically acceptable salt thereof, wherein D is —NH—C(O)—NH—, A is selected from the group consisting of substituted t-butylpyridyl group, unsubstituted t-butylpyridyl group, substituted (trifluoromethyl)pyridyl group, unsubstituted (trifluoromethyl) pyridyl group, substituted isopropylpyridyl group, unsubstituted isopropylpyridyl group, substituted (2-methyl-2-butyl)pyridyl group, unsubstituted (2-methyl-2-butyl pyridyl) group, substituted (3-methyl-3-pentyl)pyridyl group, and unsubstituted(3-methyl-3-pentyl) pyridyl groups, substituted (3-ethyl-3-pentyl)pyridyl group and unsubstituted (3-ethyl-3-pentyl)pyridyl group, A′ is a substituted isoquinolinyl group or unsubstituted isoquinolinyl group or an unsubstituted quinolinyl group, A″ is a substituted quinolinyl group, B, B′ and B″ are each, independently, a substituted or unsubstituted bridged cyclic structure of up to 30 carbon atoms of the formula -L-(ML¹)_(q) wherein L comprises a cyclic moiety having at least 5 members and is bound directly to D, L¹ comprises a cyclic moiety having at least 5 members, M is a bridging group selected from the group consisting of —O—, —S—, —N(R⁷)—, —(CH₂)_(m)—, —C(O)—, —C(OH)—, —(CH₂)_(m)O—, —(CH₂)_(m)S—, —(CH₂)_(m)N(R⁷)—, —O(CH₂)_(m), —CHX^(a)—, —CX^(a) ₂—, —S—(CH₂)_(m)— and —N(R⁷)(CH₂)_(m)—, where m=1-3, X^(a) is halogen, and R⁷ is as defined below, q is an integer of from 1-3, and each cyclic structure of L and L¹ contains 0-4 members of the group consisting of nitrogen, oxygen and sulfur, subject to the provisos that B is not

and B′ is not

wherein the substituents for A″ and the substituted isoquinolyl groups of A′ are selected from the group consisting of halogen, up to per-halo, and Wn, where n is 0-3 and each W is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, at least a five membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O; —CN, up to per halo substituted C₆-C₁₄ aryl, up to per halo substituted C₇-C₂₄ alkaryl, up to per halo substituted C₇₋₄ aralkyl, up to per halo substituted C₃-C₁₂ heteroaryl having at least 5 members and 1-3 heteratoms selected from O, N and S, up to per halo substituted C₄-C₂₄ alkylheteroaryl having at least 5 members and 1-3 heteroatoms selected from O, N and S, C₆-C₁₄ aryl, C₁-C₂₄ alkaryl, C₁-C₂₄ aralkyl, C₃-C₁₂ heteroaryl having at least 5 cyclic members and 1-3 heteroatoms selected from O, N and S, C₄-C₂₄ alkylheteroaryl having at least 5 cyclic members and 1-3 heteroatoms selected from O, N and S; —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ alkenyl and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein the substitutents for the substituted t-butyl pyridyl groups substituted trifluoromethyl pyridyl groups, substituted isopropyl pyridyl groups, substituted 2-methyl-2-butyl pyridyl groups and substituted 3-methyl-3-pentyl pyridyl groups of A are selected from the group consisting of halogen, up to per-halo, and Zn, where n is 0-3 and each Z is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W; where B and B′ are substituted, the substituents are selected from the group consisting of halogen, up to per-halo, and Jn, where n is 0-3 and each J is independently selected from the group consisting of —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, at least a five-membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, C₆₋₁₂ aryl, at least a five-membered C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, C₇₋₂₄ aralkyl, C₇₋₂₄ alkaryl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O, substituted C₆-C₁₄ aryl, at least a five-membered substituted C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, substituted C₇₋₂₄ alkaryl and substituted C₇-C₂₄ aralkyl, where B″ is substituted, the substituents are selected from the group consisting of halogen, —CN, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7″) independently as defined above for W, C₁₋₁₀ alkyl, at least a five-membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, C₆₋₁₂ aryl, at least a five-membered C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, C₇₋₂₄ aralkyl, C₇₋₂₄ alkaryl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O, substituted C₆-C₁₄ aryl, at least a five-membered substituted C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, substituted C₇₋₂₄ alkaryl and substituted C₇-C₂₄ aralkyl, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), —C(O)NR^(a)R^(b) and —SO₂R^(a) wherein each R^(a) and R^(b) are independently hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O, where J is a substituted group, it is substituted by halogen, up to per halo, or by one or more substituents independently selected from the group consisting of —CN, —CO₂R⁷, —OR⁷, —SR⁷, —NR⁷R^(7′), —NO₂, —NR⁷C(O)R^(7′) and —NR⁷C(O)OR^(7′); with each R⁷ and R^(7′) independently as defined above for W, to treat said patient.
 42. A method for the treatment of carcinomas of the lungs, pancreas, thyroid, bladder or colon, myeloid leukemia or villous colon adenoma, comprising administering a therapeutically effective amount of a compound of one of the following formulae A-D-B  (I) A′-D-B′  (II) and A″-D-B″  (III) or a pharmaceutically acceptable salt thereof, wherein D is —NH—C(O)—NH—, A is selected from the group consisting of substituted t-butylpyridyl group, unsubstituted t-butylpyridyl group, substituted (trifluoromethyl)pyridyl group, unsubstituted (trifluoromethyl) pyridyl group, substituted isopropylpyridyl group, unsubstituted isopropylpyridyl group, substituted (2-methyl-2-butyl)pyridyl group, unsubstituted (2-methyl-2-butyl pyridyl) group, substituted (3-methyl-3-pentyl)pyridyl group, and unsubstituted (3-methyl-3-pentyl) pyridyl groups, substituted (3-ethyl-3-pentyl)pyridyl group and unsubstituted (3-ethyl-3-pentyl)pyridyl group, A′ is a substituted isoquinolinyl group or unsubstituted isoquinolinyl group or an unsubstituted quinolinyl group, A″ is a substituted quinolinyl group, B, B′ and B″ are each, independently, a substituted or unsubstituted bridged cyclic structure of up to 30 carbon atoms of the formula -L-(ML¹)_(q) wherein L comprises a cyclic moiety having at least 5 members and is bound directly to D, L¹ comprises a cyclic moiety having at least 5 members, M is a bridging group selected from the group consisting of —O—, —S—, —N(R⁷)—, —(CH₂)_(m)—, —C(O)—, —C(OH)—, —(CH₂)_(m)O—, —(CH₂)_(m)S—, —(CH₂)_(m)N(R⁷)—, —O(CH₂)_(m), —CHX^(a)—, —CX^(a) ₂—, —S—(CH₂)_(m)— and —N(R⁷)(CH₂)_(m)—, where m=1-3, X^(a) is halogen, and R⁷ is as defined below, q is an integer of from 1-3, and each cyclic structure of L and L¹ contains 0-4 members of the group consisting of nitrogen, oxygen and sulfur, subject to the provisos that B is not

and B′ is not

wherein the substituents for A″ and the substituted isoquinolinyl groups of A′ are selected from the group consisting of halogen, up to per-halo, and Wn, where n is 0-3 and each W is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy. at least a five membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O; —CN, up to per halo substituted C₆-C₁₄ aryl, up to per halo substituted C₇-C₂₄ alkaryl, up to per halo substituted C₇₋₄ aralkyl, up to per halo substituted C₃-C₁₂ heteroaryl having at least 5 members and 1-3 heteratoms selected from O, N and S, up to per halo substituted C₄-C₂₄ alkylheteroaryl having at least 5 members and 1-3 heteroatoms selected from O, N and S, C₆-C₁₄ aryl, C₁-C₂₄ alkaryl, C₁-C₂₄ aralkyl, C₃-C₁₂ heteroaryl having at least 5 cyclic members and 1-3 heteroatoms selected from O, N and S, C₄-C₂₄ alkylheteroaryl having at least 5 cyclic members and 1-3 heteroatoms selected from O, N and S; —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ alkenyl and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein the substitutents for the substituted t-butyl pyridyl groups substituted trifluoromethyl pyridyl groups, substituted isopropyl pyridyl groups, substituted 2-methyl-2-butyl pyridyl groups and substituted 3-methyl-3-pentyl pyridyl groups of A are selected from the group consisting of halogen, up to per-halo, and Zn, where n is 0-3 and each Z is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W; where B and B′ are substituted, the substituents are selected from the group consisting of halogen, up to per-halo, and Jn, where n is 0-3 and each J is independently selected from the group consisting of —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, at least a five-membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, C₆₋₁₂ aryl, at least a five-membered C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, C₇₋₂₄ aralkyl, C₇₋₂₄ alkaryl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O, substituted C₆-C₁₄ aryl, at least a five-membered substituted C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, substituted C₇₋₂₄ alkaryl and substituted C₇-C₂₄ aralkyl, where B″ is substituted, the substituents are selected from the group consisting of halogen, —CN, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7″) independently as defined above for W, C₁₋₁₀ alkyl, at least a five-membered C₃₋₁₀ cycloalkyl having 0-3 heteroatoms, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, C₆₋₁₂ aryl, at least a five-membered C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, C₇₋₄ aralkyl, C₇₋₂₄ alkaryl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, at least a five-membered substituted C₃₋₁₀ cycloalkyl having 0-3 heteroatoms selected from N, S and O, substituted C₆-C₁₄ aryl, at least a five-membered substituted C₃₋₁₂ hetaryl having 1-3 heteroatoms selected from N, S and O, substituted C₇₋₂₄ alkaryl and substituted C₇-C₂₄ aralkyl, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), —C(O)NR^(a)R^(b) and —SO₂R^(a) wherein each R^(a) and R^(b) are independently hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O, where J is a substituted group, it is substituted by halogen, up to per halo, or by one or more substituents independently selected from the group consisting of —CN, —CO₂R⁷, —OR⁷, —SR⁷, —NR⁷R^(7′), —NO₂, —NR⁷C(O)R^(7′) and —NR⁷C(O)OR^(7′); with each R⁷ and R^(7′) independently as defined above for W, to treat said patient.
 43. A method as in claim 41 for the treatment of a solid tumor with cell growth mediated by raf kinase in a patient, comprising administering a therapeutically effective amount of a compound of one of the following formulae A-D-B, A′-D-B′, A″-D-B″.

R is selected from the group consisting of halogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7″), —NR⁷C(O)R^(7′), or a pharmaceutically acceptable salt thereof wherein D is —NH—C(O)—NH— A is selected from the group consisting of substituted t-butylpyridyl groups, unsubstituted t-butylpyridyl group, substituted (trifluoromethyl)pyridyl group, unsubstituted (trifluoromethyl) pyridyl group, substituted isopropylpyridyl group, unsubstituted isopropylpyridyl group, substituted (2-methyl-2-butyl)pyridyl group, unsubstituted (2-methyl-2-butyl) pyridyl group, substituted (3-methyl-3-pentyl) pyridyl group, unsubstituted (3-methyl-3-pentyl) pyridyl group, substituted (3-ethyl-3-pentyl)pyridyl group, unsubstituted (3-ethyl-3-pentyl) pyridyl group, A′ is a substituted isoquinolinyl group or unsubstituted isoquinolinyl group or an unsubstituted quinolinyl group, A″ is a substituted quinolinyl group, B, B′ and B″ are each independently of the formula -L-(ML¹)_(q), wherein L is phenyl or substituted phenyl and L¹ is phenyl, substituted phenyl, pyridinyl or substituted pyridinyl, q is an integer of from 1-2 and M is selected from the group consisting of —O—, —S—, —N(R⁷)—, —(CH₂)_(m)—, —C(O)—, —CH(OH)—, —(CH₂)_(m)O—, —(CH₂)_(m)S—, —(CH₂)_(m)N(R⁷)—, —O(CH₂)_(m), CHX^(a)—, CX^(a) ₂—, —S—(CH₂)— and —N(R⁷)(CH₂)_(m)—, where m=1-3, X^(a) is halogen, and R⁷ is as defined below; subject to the provisos that B′ is not

B is not

wherein the substituents for the substituted t-butyl pyridyl groups, substituted trifluoromethyl pyridyl groups, substituted isopropyl pyridyl groups, substituted 2-methylbutyl pyridyl groups and 3-methylpentyl pyridyl groups, of A are selected from the group consisting of halogen, up to per-halo, and Zn, where n is 0-3 and each Z is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₁₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein the substituents for A″ and the substituted isoquinolinyl groups of A′ are selected from the group consisting of halogen, up to per-halo, and Wn, where n is 0-3 and each W is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ alkenyl and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein B and B′ are substituted, the substituents are selected from the group consisting of halogen, up to per-halo, and Jn, where n is 0-3 and each J is independently selected from the group consisting of —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, and substituted C₁₋₁₀ alkoxy, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), —C(O)NR^(a)R^(b) and —SO₂R^(a) wherein R^(a) and R^(b) are each independently hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O, wherein B″ is substituted, the substituents are selected from the group consisting of halogen, —CN, —C(O)NR⁷R^(7′), —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, and substituted C₁₋₁₀ alkoxy, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), C(O)NR^(a)R^(b) and —SO₂R^(a) wherein R^(a) and R^(b) are each independently, hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O to a patient in need thereof.
 44. (canceled)
 45. A method as in claim 42 for the treatment of carcinomas of the lungs, pancreas, thyroid, bladder or colon, myeloid leukemia or villous colon adenoma in a patient mediated by raf kinase, comprising administering a therapeutically effective amount of a compound of one of the following formulae A-D-B, A′-D-B′, A″-D-B″,

R is selected from the group consisting of halogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7″), —NR⁷C(O)R^(7′), or a pharmaceutically acceptable salt thereof wherein D is —NH—C(O)—NH— A is selected from the group consisting of substituted t-butylpyridyl groups, unsubstituted t-butylpyridyl group, substituted (trifluoromethyl)pyridyl group, unsubstituted (trifluoromethyl) pyridyl group, substituted isopropylpyridyl group, unsubstituted isopropylpyridyl group, substituted (2-methyl-2-butyl)pyridyl group, unsubstituted (2-methyl-2-butyl) pyridyl group, substituted (3-methyl-3-pentyl) pyridyl group, unsubstituted (3-methyl-3-pentyl) pyridyl group, substituted (3-ethyl-3-pentyl)pyridyl group, unsubstituted (3-ethyl-3-pentyl) pyridyl group, A′ is a substituted isoquinolinyl group or unsubstituted isoquinolinyl group or an unsubstituted quinolinyl group, A″ is a substituted quinolinyl group, B, B′ and B″ are each independently of the formula -L-(ML¹)_(q), wherein L is phenyl or substituted phenyl and L¹ is phenyl, substituted phenyl, pyridinyl or substituted pyridinyl, q is an integer of from 1-2 and M is selected from the group consisting of —O—, —S—, —N(R⁷)—, —(CH₂)_(m)—, —C(O)—, —CH(OH)—, —(CH₂)_(m)O—, —(CH₂)_(m)S—, —(CH₂)_(m)N(R⁷)—, —O(CH₂)_(m), CHX^(a)—, CX^(a) ₂—, —S—(CH₂)— and —N(R⁷)(CH₂)_(m)—, where m=1-3, X^(a) is halogen, and R⁷ is as defined below; subject to the provisos that B′ is not

B is not

wherein the substituents for the substituted t-butyl pyridyl groups, substituted trifluoromethyl pyridyl groups, substituted isopropyl pyridyl groups, substituted 2-methylbutyl pyridyl groups and 3-methylpentyl pyridyl groups, of A are selected from the group consisting of halogen, up to per-halo, and Zn, where n is 0-3 and each Z is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein the substituents for A″ and the substituted isoquinolinyl groups of A′ are selected from the group consisting of halogen, up to per-halo, and Wn, where n is 0-3 and each W is independently selected from the group consisting of C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, substituted C₁₋₁₀ alkoxy, —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently selected from hydrogen, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, up to per halosubstituted C₁₋₁₀ alkyl, up to per halosubstituted C₁₋₁₀ alkoxy, up to per halosubstituted C₂₋₁₀ alkenyl and up to per halosubstituted C₁₋₁₀ alkenoyl; wherein B and B′ are substituted, the substituents are selected from the group consisting of halogen, up to per-halo, and Jn, where n is 0-3 and each J is independently selected from the group consisting of —CN, —CO₂R⁷, —C(O)NR⁷R^(7′), —C(O)—R⁷, —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₁₋₁₀ alkoxy, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, and substituted C₁₋₁₀ alkoxy, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), —C(O)NR^(a)R^(b) and —SO₂R^(a) wherein R^(a) and R^(b) are each independently hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O, wherein B″ is substituted, the substituents are selected from the group consisting of halogen, —CN, —C(O)NR⁷R^(7′), —NO₂, —OR⁷, —SR⁷, —NR⁷R^(7′), —NR⁷C(O)OR^(7′), —NR⁷C(O)R^(7′), with each R⁷ and R^(7′) independently as defined above for W, C₁₋₁₀ alkyl, C₂₋₁₀ alkenyl, C₁₋₁₀ alkenoyl, substituted C₁₋₁₀ alkyl, and substituted C₁₋₁₀ alkoxy, subject to the proviso that where B, B′ or B″ is -L(ML¹)_(q), L¹ is not substituted by the substituents —C(O)R^(a), —C(NR^(a))R^(b), C(O)NR^(a)R^(b) and —SO₂R^(a) wherein R^(a) and R^(b) are each independently, hydrogen or a carbon based moiety of up to 24 carbon atoms, optionally containing heteroatoms selected from N, S and O to treat said patient.
 46. A method as in claim 41 for the treatment of a solid tumor with cell growth mediated by raf kinase in a patient, comprising administering a therapeutically effective amount of a compound which is N-(4-tert-butylpyridinyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-phenoxyphenyl)urea or a pharmaceutically acceptable salt thereof: N-(4-tert-butylpyridinyl)-N′-(4-(4-methylphenoxy)phenyl) or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-chlorophenoxy)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-pyridinyloxy)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-pyridinylthio)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(3-(4-pyridinylthio)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(3-isoquinolinyl)-N′-(4-(4-pyridinyloxy)phenyl) urea or a pharmaceutically acceptable salt thereof; N,N′-(bis(3-(2-methoxyquinolinyl)) urea) or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinylmethyl)phenyl)) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinylcarbonyl)phenyl)) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinyloxy)phenyl))urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-((4-methoxyphenyl)methylamino)phenyl) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(3-(4-pyridinylthio)phenyl)) urea or a pharmaceutically acceptable salt thereof; or N-(1-(4-methylpiperazinyl)-3-isoquinolinyl)-N′ (4-(4-pyridinyloxy)phenyl)urea or a pharmaceutically acceptable salt thereof, to treat said patient.
 47. A method as in claim 42 for the treatment of carcinomas of the lungs, pancreas, thyroid, bladder or colon, myeloid leukemia or villous colon adenoma, comprising administering a therapeutically effective amount of a compound which is N-(4-tert-butylpyridinyl)-N′-(4-(4-pyridinylmethyl)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-phenoxyphenyl) urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-methylphenoxy)phenyl) or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-chlorophenoxy)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-pyridinyloxy)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(4-(4-pyridinylthio)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(4-tert-butylpyridinyl)-N′-(3-(4-pyridinylthio)phenyl)urea or a pharmaceutically acceptable salt thereof; N-(3-isoquinolinyl)-N′-(4-(4-pyridinyloxy phenyl)urea or a pharmaceutically acceptable salt thereof; N,N′-(bis(3-(2-methoxy-quinolinyl))urea) or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinylmethyl)-phenyl)) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinylcarbonyl)phenyl)) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-(4-pyridinyloxy)phenyl)) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(4-((4-methoxyphenyl)methylamino)phenyl)) urea or a pharmaceutically acceptable salt thereof; N-(3-(2-methoxyquinolinyl)-N′-(3-(4-pyridinylthio)phenyl)) urea or a pharmaceutically acceptable salt thereof; or N-(1-(4-methylpiperazinyl)-3-isoquinolinyl)-N′ (4-(4-pyridinyloxy)phenyl)urea or a pharmaceutically acceptable salt thereof to treat said patient.
 48. A method as in claim 47 for the treatment of carcinomas of the lungs.
 49. A method as in claim 47 for the treatment of carcinomas of the pancreas.
 50. A method as in claim 47 for the treatment of carcinomas of the thyroid.
 51. A method as in claim 47 for the treatment of carcinomas of the bladder.
 52. A method as in claim 47 for the treatment of carcinomas of the colon.
 53. A method as in claim 47 for the treatment of myeloid leukemia.
 54. A method as in claim 47 for the treatment of villous colon adenoma. 